•Неизползвайтеоборудването, преди да сте се консултирали иразбралиупътванетозаработа.
•Неспазването на това предупреждение може да доведе до
нараняване на
резултат на токов удар, механична или друга опасност.
本维修手册仅提供英文版本。
• 如果客户的维修服务人员需要非英文版本,则客户需自行提供翻译服
务。
• 未详细阅读和完全理解本维修手册之前,不得进行维修。
• 忽略本警告可能对维修服务人员、操作人员或患者造成电击、机械伤害
或其他形式的伤害。
本服務手冊僅提供英文版本。
•倘若客戶的服務供應商需要英文以外之服務手冊,客戶有責任提供翻譯
服務。
•除非已參閱本服務手冊及明白其內容,否則切勿嘗試維修設備。
•不遵從本警告或會令服務供應商、網絡供應商或病人受到觸電、機械性
或其他的危險。
本維修手冊僅有英文版。
•若客戶的維修廠商需要英文版以外的語言,應由客戶自行提供翻譯服
務。
•請勿試圖維修本設備,除非 您已查閱並瞭解本維修手冊。
•若未留意本警告,可能導致維修廠商、操作員或病患因觸電、機械或其
他危險而受傷。
доставчиканауслугата, оператораилипациентa в
UPOZORENJE
(HR)
VÝSTRAHA
(CS)
Ovaj servisni priručnik dostupan je na engleskom jeziku.
•Ako davatelj usluge klijenta treba neki drugi jezik, klijent je dužan
osigurati prijevod.
•Ne pokušavajte servisirati opremu ako niste u potpunosti pročitali i
razumjeli ovaj servisni priručnik.
•Zanemarite li ovo upozorenje, može doći do ozljede davatelja usluge,
operatera ili pacijenta uslijed strujnog udara, mehaničkih ili drugih rizika.
Tento provozní návod existuje pouze v anglickém jazyce.
•V případě, že externí služba zákazníkům potřebuje návod v jiném
jazyce, je zajištění překladu do odpovídajícího jazyka úkolem
zákazníka.
•Nesnažte se o údržbu tohoto zařízení, aniž byste si přečetli tento
provozní návod a pochopili jeho obsah.
•V případě nedodržování této výstrahy může dojít k poranění pracovníka
prodejního servisu, obslužného personálu nebo pacientů vlivem
elektrického proudu, respektive vlivem mechanických či jiných rizik.
•Hvis en kundes tekniker har brug for et andet sprog end engelsk, er det
kundens ansvar at sørge for oversættelse.
•Forsøg ikke at servicere udstyret uden at læse og forstå denne
servicemanual.
•Manglende overholdelse af denne advarsel kan medføre skade på
grund af elektrisk stød, mekanisk eller anden fare for teknikeren,
operatøren eller patienten.
Deze onderhoudshandleiding is enkel in het Engels verkrijgbaar.
•Als het onderhoudspersoneel een andere taal vereist, dan is de klant
verantwoordelijk voor de vertaling ervan.
•Probeer de apparatuur niet te onderhouden alvorens deze
onderhoudshandleiding werd geraadpleegd en begrepen is.
•Indien deze waarschuwing niet wordt opgevolgd, zou het
onderhoudspersoneel, de operator of een patiënt gewond kunnen raken
als gevolg van een elektrische schok, mechanische of andere gevaren.
This service manual is available in English only.
•If a customer's service provider requires a language other than english,
it is the customer's responsibility to provide translation services.
•Do not attempt to service the equipment unless this service manual has
been consulted and is understood.
•Failure to heed this warning may result in injury to the service provider,
operator or patient from electric shock, mechanical or other hazards.
HOIATUS
(ET)
VAROITUS
(FI)
ATTENTION
(FR)
See teenindusjuhend on saadaval ainult inglise keeles
•Kui klienditeeninduse osutaja nõuab juhendit inglise keelest erinevas
keeles, vastutab klient tõlketeenuse osutamise eest.
•Ärge üritage seadmeid teenindada enne eelnevalt käesoleva
teenindusjuhendiga tutvumist ja sellest aru saamist.
•Käesoleva hoiatuse eiramine võib põhjustada teenuseosutaja,
operaatori või patsiendi vigastamist elektrilöögi, mehaanilise või muu
ohu tagajärjel.
Tämä huolto-ohje on saatavilla vain englanniksi.
•Jos asiakkaan huoltohenkilöstö vaatii muuta kuin englanninkielistä
materiaalia, tarvittavan käännöksen hankkiminen on asiakkaan
vastuulla.
•Älä yritä korjata laitteistoa ennen kuin olet varmasti lukenut ja
ymmärtänyt tämän huolto-ohjeen.
•Mikäli tätä varoitusta ei noudateta, seurauksena voi olla
huoltohenkilöstön, laitteiston käyttäjän tai potilaan vahingoittuminen
sähköiskun, mekaanisen vian tai muun vaaratilanteen vuoksi.
Ce manuel d’installation et de maintenance est disponible uniquement en
anglais.
•Si le technicien d'un client a besoin de ce manuel dans une langue
autre que l'anglais, il incombe au client de le faire traduire.
•Ne pas tenter d'intervenir sur les équipements tant que ce manuel
d’installation et de maintenance n'a pas été consulté et compris.
•Le non-respect de cet avertissement peut entraîner chez le technicien,
l'opérateur ou le patient des blessures dues à des dangers électriques,
mécaniques ou autres.
Diese Serviceanleitung existiert nur in englischer Sprache.
•Falls ein fremder Kundendienst eine andere Sprache benötigt, ist es
Aufgabe des Kunden für eine entsprechende Übersetzung zu sorgen.
•Versuchen Sie nicht diese Anlage zu warten, ohne diese
Serviceanleitung gelesen und verstanden zu haben.
•Wird diese Warnung nicht beachtet, so kann es zu Verletzungen des
Kundendiensttechnikers, des Bedieners oder des Patienten durch
Stromschläge, mechanische oder sonstige Gefahren kommen.
Τοπαρόνεγχειρίδιοσέρβιςδιατίθεταιμόνοστααγγλικά.
•Εάνοτεχνικόςσέρβιςενόςπελάτη απαιτεί το παρόν εγχειρίδιο σε
γλώσσα εκτός των αγγλικών, αποτελεί ευθύνη του πελάτη να παρέχει
τις υπηρεσίες μετάφρασης.
•Μην επιχειρήσετε την εκτέλεση εργασιών σέρβις στον εξοπλισμό αν δεν
έχετε συμβουλευτεί και κατανοήσει το παρόν εγχειρίδιο
•Αν δεν προσέξετε την προειδοποίηση αυτή, ενδέχεται να προκληθεί
τραυματισμός στον τεχνικό σέρβις, στο χειριστή ή στον ασθενή από
ηλεκτροπληξία, μηχανικούς ή άλλους κινδύνους.
Ezen karbantartási kézikönyv kizárólag angol nyelven érhető el.
•Ha a vevő szolgáltatója angoltól eltérő nyelvre tart igényt, akkor a vevő
felelőssége a fordítás elkészíttetése.
•Ne próbálja elkezdeni használni a berendezést, amíg a karbantartási
kézikönyvben leírtakat nem értelmezték.
•Ezen figyelmeztetés figyelmen kívül hagyása a szolgáltató, működtető
vagy a beteg áramütés, mechanikai vagy egyéb veszélyhelyzet miatti
sérülését eredményezheti.
σέρβις.
AÐVÖRUN
(IS)
AVVERTENZA
(IT)
警告
(JA)
Þessi þjónustuhandbók er aðeins fáanleg á ensku.
•Ef að þjónustuveitandi viðskiptamanns þarfnast annas tungumáls en
ensku, er það skylda viðskiptamanns að skaffa tungumálaþjónustu.
•Reynið ekki að afgreiða tækið nema að þessi þjónustuhandbók hefur
verið skoðuð og skilin.
•Brot á sinna þessari aðvörun getur leitt til meiðsla á þjónustuveitanda,
stjórnanda eða sjúklings frá raflosti, vélrænu eða öðrum áhættum.
Il presente manuale di manutenzione è disponibile soltanto in lingua
inglese.
•Se un addetto alla manutenzione richiede il manuale in una lingua
diversa, il cliente è tenuto a provvedere direttamente alla traduzione.
•Procedere alla manutenzione dell'apparecchiatura solo dopo aver
consultato il presente manuale ed averne compreso il contenuto.
•Il mancato rispetto della presente avvertenza potrebbe causare lesioni
all'addetto alla manutenzione, all'operatore o ai pazienti provocate da
scosse elettriche, urti meccanici o altri rischi.
• 고객의 서비스 제공자가 영어 이외의 언어를 요구할 경우 , 번역 서비스
를 제공하는 것은 고객의 책임입니다 .
• 본 서비스 매뉴얼을 참조하여 숙지하지 않은 이상 해당 장비를 수리하
려고 시도하지 마십시오 .
• 본 경고 사항에 유의하지 않으면 전기 쇼크 , 기계적 위험 , 또는 기타 위
험으로 인해 서비스 제공자 , 사용자 또는 환자에게 부상을 입힐 수 있
습니다 .
Šī apkopes rokasgrāmata ir pieejama tikai angļu valodā.
•Ja klienta apkopes sniedzējam nepieciešama informācija citā valodā,
klienta pienākums ir nodrošināt tulkojumu.
•Neveiciet aprīkojuma apkopi bez apkopes rokasgrāmatas izlasīšanas
un saprašanas.
•Šī brīdinājuma neievērošanas rezultātā var rasties elektriskās strāvas
trieciena, mehānisku vai citu faktoru izraisītu traumu risks apkopes
sniedzējam, operatoram vai pacientam.
Šis eksploatavimo vadovas yra tik anglų kalba.
•Jei kliento paslaugų tiekėjas reikalauja vadovo kita kalba – ne anglų,
suteikti vertimo paslaugas privalo klientas.
•Nemėginkite atlikti įrangos techninės priežiūros, jei neperskaitėte ar
nesupratote šio eksploatavimo vadovo.
•Jei nepaisysite šio įspėjimo, galimi paslaugų tiekėjo, operatoriaus ar
paciento sužalojimai dėl elektros šoko, mechaninių ar kitų pavojų.
ADVARSEL
(NO)
OSTRZEŻENIE
(PL)
ATENÇÃO
(PT-BR)
Denne servicehåndboken finnes bare på engelsk.
•Hvis kundens serviceleverandør har bruk for et annet språk, er det
kundens ansvar å sørge for oversettelse.
•Ikke forsøk å reparere utstyret uten at denne servicehåndboken er lest
og forstått.
•Manglende hensyn til denne advarselen kan føre til at
serviceleverandøren, operatøren eller pasienten skades på grunn av
elektrisk støt, mekaniske eller andre farer.
Niniejszy podręcznik serwisowy dostępny jest jedynie w języku angielskim.
•Jeśli serwisant klienta wymaga języka innego niż angielski,
zapewnienie usługi tłumaczenia jest obowiązkiem klienta.
•Nie próbować serwisować urządzenia bez zapoznania się z niniejszym
podręcznikiem serwisowym i zrozumienia go.
•Niezastosowanie się do tego ostrzeżenia może doprowadzić do
obrażeń serwisanta, operatora lub pacjenta w wyniku porażenia prądem
elektrycznym, zagrożenia mechanicznego bądź innego.
Este manual de assistência técnica encontra-se disponível unicamente em
inglês.
•Se outro serviço de assistência técnica solicitar a tradução deste
manual, caberá ao cliente fornecer os serviços de tradução.
•Não tente reparar o equipamento sem ter consultado e compreendido
este manual de assistência técnica.
•A não observância deste aviso pode ocasionar ferimentos no técnico,
operador ou paciente decorrentes de choques elétricos, mecânicos ou
outros.
Este manual de assistência técnica só se encontra disponível em inglês.
•Se qualquer outro serviço de assistência técnica solicitar este manual
noutro idioma, é da responsabilidade do cliente fornecer os serviços de
tradução.
•Não tente reparar o equipamento sem ter consultado e compreendido
este manual de assistência técnica.
•O não cumprimento deste aviso pode colocar em perigo a segurança
do técnico, do operador ou do paciente devido a choques eléctricos,
mecânicos ou outros.
Acest manual de service este disponibil doar în limba engleză.
•Dacă un furnizor de servicii pentru clienţi necesită o altă limbă decât
cea engleză, este de datoria clientului să furnizeze o traducere.
•Nu încercaţi să reparaţi echipamentul decât ulterior consultării şi
înţelegerii acestui manual de service.
•Ignorarea acestui avertisment ar putea duce la rănirea depanatorului,
operatorului sau pacientului în urma pericolelor de electrocutare,
mecanice sau de altă natură.
Данное руководство по техническому обслуживанию представлено
только на английском языке.
•Если сервисному персоналу клиента необходимо руководство не
на английском, а на каком-то другом языке, клиенту следует
самостоятельно обеспечить перевод.
•Перед техническим обслуживанием оборудования обязательно
обратитесь к данному руководству и поймите изложенные в нем
сведения.
•Несоблюдение требований данного предупреждения
привести к тому, что специалист по техобслуживанию, оператор
или пациент получит удар электрическим током, механическую
травму или другое повреждение.
может
UPOZORENJE
(SR)
UPOZORNENIE
(SK)
Ovo servisno uputstvo je dostupno samo na engleskom jeziku.
•Ako klijentov serviser zahteva neki drugi jezik, klijent je dužan da
obezbedi prevodilačke usluge.
•Ne pokušavajte da opravite uređaj ako niste pročitali i razumeli ovo
servisno uputstvo.
•Zanemarivanje ovog upozorenja može dovesti do povređivanja
servisera, rukovaoca ili pacijenta usled strujnog udara ili mehaničkih i
drugih opasnosti.
Tento návod na obsluhu je k dispozícii len v angličtine.
•Ak zákazníkov poskytovateľ služieb vyžaduje iný jazyk ako angličtinu,
poskytnutie prekladateľských služieb je zodpovednosťou zákazníka.
•Nepokúšajte sa o obsluhu zariadenia, kým si neprečítate návod na
obluhu a neporozumiete mu.
•Zanedbanie tohto upozornenia môže spôsobiť zranenie poskytovateľa
služieb, obsluhujúcej osoby alebo pacienta elektrickým prúdom,
mechanické alebo iné ohrozenie.
•Si el encargado de mantenimiento de un cliente necesita un idioma que
no sea el inglés, el cliente deberá encargarse de la traducción del
manual.
•No se deberá dar servicio técnico al equipo, sin haber consultado y
comprendido este manual de servicio.
•La no observancia del presente aviso puede dar lugar a que el
proveedor de servicios, el operador o el paciente sufran lesiones
provocadas por causas eléctricas, mecánicas o de otra naturaleza.
Den här servicehandboken finns bara tillgänglig på engelska. .
•Om en kunds servicetekniker har behov av ett annat språk än engelska,
ansvarar kunden för att tillhandahålla översättningstjänster.
•Försök inte utföra service på utrustningen om du inte har läst och förstår
den här servicehandboken.
•Om du inte tar hänsyn till den här varningen kan det resultera i skador
på serviceteknikern, operatören eller patienten till följd av elektriska
stötar, mekaniska faror eller andra faror.
Ta servisni priročnik je na voljo samo v angleškem jeziku.
•Če ponudnik storitve stranke potrebuje priročnik v drugem jeziku, mora
stranka zagotoviti prevod.
•Ne poskušajte servisirati opreme, če tega priročnika niste v celoti
prebrali in razumeli.
•Če tega opozorila ne upoštevate, se lahko zaradi električnega udara,
mehanskih ali drugih nevarnosti poškoduje ponudnik storitev, operater
ali bolnik.
DIKKAT
(TR)
Bu servis kılavuzunun sadece ingilizcesi mevcuttur.
•Eğer müşteri teknisyeni bu kılavuzu ingilizce dışında bir başka lisandan
talep ederse, bunu tercüme ettirmek müşteriye düşer.
All packages should be closely examined at time of delivery. If damage is apparent, have notation
"damage in shipment" written on all copies of the freight or express bill before delivery is accepted
or "signed for" by a General Electric representative or a hospital receiving agent. Whether noted or
concealed, damage MUST be reported to the carrier immediately upon discovery, or in any event,
within 14 days after receipt, and the contents and containers held for inspection by the carrier. A
transportation company will not pay a claim for damage if an inspection is not requested within this
14 day period.
To file a report:
•Call 1-800-548-3366 and use option 8.
•Fill out a report on http://egems.med.ge.com/edq/home.jsp
•Contact your local service coordinator for more information on this process.
Rev. June 13, 2006
CERTIFIED ELECTRICAL CONTRACTOR STATEMENT
All electrical Installations that are preliminary to positioning of the equipment at the site prepared for
the equipment shall be performed by licensed electrical contractors. In addition, electrical feeds into
the Power Distribution Unit shall be performed by licensed electrical contractors. Other connections
between pieces of electrical equipment, calibrations and testing shall be performed by qualified GE
Medical personnel. The products involved (and the accompanying electrical installations) are highly
sophisticated, and special engineering competence is required. In performing all electrical work on
these products, GE will use its own specially trained field engineers. All of GE’s electrical work on
these products will comply with the requirements of the applicable electrical codes.
The purchaser of GE equipment shall only utilize qualified personnel (i.e., GE’s field engineers,
personnel of third-party service companies with equivalent training, or licensed electricians) to
perform electrical servicing on the equipment.
IMPORTANT...X-RAY PROTECTION
X-ray equipment if not properly used may cause injury. Accordingly, the instructions herein
contained should be thoroughly read and understood by everyone who will use the equipment
before you attempt to place this equipment in operation. The General Electric Company, Medical
Systems Group, will be glad to assist and cooperate in placing this equipment in use.
Although this apparatus incorporates a high degree of protection against x-radiation other than the
useful beam, no practical design of equipment can provide complete protection. Nor can any
practical design compel the operator to take adequate precautions to prevent the possibility of any
persons carelessly exposing themselves or others to radiation.
It is important that anyone having anything to do with x-radiation be properly trained and fully
acquainted with the recommendations of the National Council on Radiation Protection and
Measurements as published in NCRP Reports available from NCRP Publications, 7910 Woodmont
Avenue, Room 1016, Bethesda, Maryland 20814, and of the International Commission on Radiation
Protection, and take adequate steps to protect against injury.
The equipment is sold with the understanding that the General Electric Company, Medical Systems
Group, its agents, and representatives have no responsibility for injury or damage which may result
from improper use of the equipment.
Various protective materials and devices are available. It is urged that such materials or devices be
used.
Danger of explosion if battery is incorrectly replaced. Replace only with the same or
equivalent type recommended by the manufacturer. Discard used batteries according to the
manufacturer’s instructions.
Il y a danger d’explosion s’il y a replacement incorrect de la batterie. Remplacer uniquement
avec une batterie du même type ou d’un type recommandé par le constructeur. Mettre au
rébut les batteries usagées conformément aux instructions du fabricant.
OMISSIONS & ERRORS
Customers, please contact your GE Sales or Service representatives.
GE personnel, please use the GEMS CQA Process to report all omissions, errors, and defects in
Chapter 7, Section 1.0: Added Rigging statement according to global
requirement
Chapter 1:
added floor template (P/N5341997) for GT1700 Table in Section 1.0
added Pre-installation Block Diagram in Section 3.0
Updated the EMC standard description in Section 4.0
Chapter 2:
added floor template (P/N5341997) for GT1700 Table in Section 6.0
Chapter 3: updated option list in Section 1.0
Chapter 4:
Changed Balance Weight kit to 33kg.
Added the illustrations of BSD Elite Gantry and Table in Section 6.1
added TIO and NIO16 console illustration in Section 6.3.
Added Illustrations of Freedom Workspace Table (Narrow) (part 5168666-3) and
Freedom Workspace Table (Wide) (part 5168666-2) in Section 6.4.
Updated Section 7.1 and 7.2 System Operation.
Added the cradle carrying capability of 227kg (GT1700 Table) in Section 8.0
Added illustrations of NIO16 and TIO console rear bulkhead in Section 9.0.
Added Section 11.0 Patient Environment.
Chapter 5:
added Section 5.0 System Component Noise Levels.
Updated the cooling requirement table in Section 2.0
Updated Figure 5-1 Sample Room Layout, showing approximate EMI requirements
Section 4.0
Chapter 6:
updated floor loading specification table in Section 1.0.
added GT1700 table illustration in Section 2.0.
Updated Table 6-2 Gantry and Table Mounting Requirements in Section 2.0
Added Seismic Mounting illustrations of FWS, TIO and NIO16 console in Section 2.0.
Added a warning and note in Section 2.0.
Chapter 7:
Added a column of Weight in Table 7-1 Size of Gantry & Dollies, with and without Side
Rails in Section 7.0
added GT1700 Table dimensions with dolly in Section 8.0
added TIO and NIO16 console shipment considerations in Section 9.0
Chapter 9:
Added Section 8.0 Recommended Power Distribution System (For Europe)
Added the tables of GEMS supplied cables (Standard Run) for TIO and NIO16 in
Section 3.0.
Added the tables of Extended cables for TIO and NIO16 in Section 3.0.
Added the System Interconnect Diagrams with TIO and NIO16 Console in Section 3.0
Added the tables of Supplied cables (Long Run) for TIO and NIO16 in Section 3.0.
Added the Fuse Kit table for BSD Meri (2385412-4 BOM, rev 2) in Section 5.0
Updated Table 9-9 BrightSpeed Series Partial UPS Back-up Options in Section 6.0.
Appendix: Deleted the appendix "CT Installation Site Ready Form" and added
"Alternate Cover Removal Options"
Chapter 6: Updated FLoor Levelness Requirement
Chapter 8: Added Warning Message on Section 2.2 and 3.0
1111/04/08Chapter 3: updated option list in Section 1.0
Chapter 4: added new FWS Table (part 5168666) illustration in Section 6.4
Section 7.0 updated Injector AC power cable.
Section 8.0 updated Floor Levelness
Chapter 5: Added the Notice for environmental requirement at beginning of Section 1.0
Section 1.1: Updated Temperature (Scan Room & Control Room) according to SRS
requirement.
Section 3.0: Updated Altitude values accroding to SRS requirement.
Section 4.0 updated Figure 5-1 of EMI requirement
Chapter 6: updated floor loading specification in Section 1.0
added FWS seismic info in section 2.0
Chapter 8, section 4.0: updated Figure 8-1 System Ground Map
Chapter 9, section 3.0: updated System Interconnect Diagram
Section 3.4: updated table of GEMS Supplied Cables for Options
Section 5.0 Updated the Fuse Kit BOM
1012/03/07Important Precautions: updated content for Damage In Transportation
Chapter 4: updated gantry width
Section 2.1.2 updated Regulated Minimum Working Clearance by Major Subsystem
Section 6.4 updated for FWS Seismic information
Added note to Section 8.4 Floor levelness
Added network specs to Section 9.0 Network Connections
Chapter 5: Section 4.0 added note
Section 4.2 added EMI of color monitor
Chapter 6: updated gantry width
Chapter 9: added LOTO requires to Section 7.1 Primary Power Disconnect
98/13/07Updated measurements to metric to meet European standards and
compliance. General revision of manual.
Important Precautions: updated by adding Bulgarian warnings
Chapter 4:
Added Section 8.7: Ceiling Requirement
Removed FWS extended cables Table to Chapter 9, Section 3.2
This direction contains physical and electrical data necessary for planning and preparing a site.
Pre-installation work is defined as site preparation for installation of the GE CT scanner. It is the
responsibility of the purchaser to arrange and pay for this work. Pre-installation work includes:
•Installation of electrical conduit, junction boxes, ducts, outlets, and line safety switches.
•Installation of interconnection wiring that is AWG stranded copper. The electrical contractor shall
ring out and tag all wires at both ends. Color-coded wires are recommended for easier identifi
cation. Wires shall be continuous without splices. Ground wires must conform to local codes.
•Any site renovation.
•Alterations and modifications to products not specifically included in the sales contract.
All work must conform to local building and safety codes. Unless specifically mentioned, GE
Healthcare does not provide or install wires, conduits, junction boxes, and ducts as illustrated in this
publication.
All CT site plans, preliminary concepts and final working drawings must be reviewed by General
Electric Headquarters Architectural Planning prior to construction or approval.
Contact your local General Electric sales representative for complete information regarding your
site-specific room layout.
-
Section 1.0
Site Readiness
Site ready is a requirement that must be achieved to install a CT product. For your convenience, a
site ready visit inspection shall be performed at least three (3) days prior to the installation date. The
site inspection must conclude with a minimum of a conditional pass status to be ready on the
requested installation delivery date. Site ready inspections on the delivery date will not be
acceptable unless prior arrangements have been made.
Pre-Installation and Site Ready Tools:
•Floor template for BrightSpeed with H-Power Table (P/N 5160024)
•Floor template for BrightSpeed with GT1700 Table (P/N 5341997)
The CT air intake is near the bottom of the gantry. Fine dust as listed below will be deposited
throughout the gantry, table, console and PDU electronics. This fine dust cannot be completely
removed and can be damaging to electronic components.
For these reasons, the scanner should be the last item installed in your CT suite area.
“Pre-installation” is work necessary to plan and prepare a site for installation of equipment.
Pre-installation work helps the user (customer) avoid:
•Application delay and scheduling
•Surprise siting discoveries
•Installation confusion
•Waste of manpower
The following MUST be completed before installation work can begin for a GE CT scanner:
•Completely finished:
-Wall painted or have final wall covering
-Ceiling tiles installed and no remaining ceiling work is required
-Final floors covering installed with no remaining dust causing floor work required
-All room millwork installed as shown on the site print
-All plumbing work in the CT suite is completed
-No construction in or around the scan suite AREA that will produce:
*Concrete dust
*Drywall dust
*Ceiling tile dust
*Wood sawdust or shaving
*Dust tracked into the CT suite area
•Active Broad Band connection
-A completed network connection is required for ALL CT installations.
-A GE Healthcare network specialist may be required to complete the VPN connection.
This may take a week or longer to schedule.
•Power available to A1, with provision for Lockout/Tagout at the A1 disconnect
If a UPS is required, a GE A1 breaker* will be needed to complete this installation. Refer
to the electrical section for more details.
NOTICE SERVICE NOTICE: An improperly prepared site (i.e., one that is in a state of construction)
can result in increased installation time.
A CT scanner installed in a dirty environment is more prone to contamination, which can
result in decreased reliability and increased scanner downtime.
This list below will describe many of the items to consider when planning for a system replacement
or designing a room for new equipment
•Determine room dimensions and verify that doorways are large enough for the scanner system.
•Install appropriate conduits and duct work for system cables. If additional components are
required in the CT suite, their connection consideration must be determined and completed.
•Install junction boxes of correct size with covers at locations shown in installation plan.
•A1 main disconnect installation
•Install power supply of correct voltage output and adequate KVA rating.
•Install local disconnects, including proper over-current protection.
•Install “steelwork” or other suitable support work for mounting equipment on walls or from
ceiling.
•Camera should be on-site at the time of installation.
•Complete all suite and room alterations and modifications.
•Verify that room shielding is adequate for the system being installed
•Review structural requirement - including floor vibration, levelness, and thickness
•Review HVAC requirements including system regulation and patient comfort.
•Review operational clearances to see if your daily used items fit, such as beds and carts.
•Emergency medical equipment should also be considered
•Storage cabinets and sink (if required) must be shown on the site print
•These contractors and others may be required to help confirm that the site meet all installation
requirements:
-Structural Engineer and /or Architect
-HVAC contractor
-Electrical contractor
-Qualified radiological health physicist
The above items can be found in chapter 2 through 9 in this manual.
It is suggested that this work be completed at least three days prior to delivery
1 – Intoduction
2.3Manufacturer’s System Level Siting Requirements
These siting requirements are the minimum that must be met in order to install a new or replacement
system.
•Network Communication in place and active
•Meets all scan room regulatory and service requirements
•Meets all minimum scan room structural requirements
•Meets minimum scan room HVAC requirements
•Meets minimum scan room electrical requirements
•Reviewed radiation protection section in the Pre-Installation manual
•All in room items shown on the final GE Healthcare site print and the final print is on site
•No construction in the scan room or neighboring suite areas
It is suggested that this work be completed at least three days prior to delivery
The site ready visit will take place at least three days prior to the delivery date. The site ready visit
is intended to verify that all of the siting requirement are met and the site is ready for installation.
The site ready visit will result in a report to the project manager indicating one of the following:
Pass - All required items are present, completed and the site is ready for installation.
Conditional Pass - is issued when 80% of all of the task are completed and all parties
agree that the 20% will be completed by the installation delivery date.
If a “Conditional Pass” is granted on the inspection date, the project manager must present
conclusive evidence that unfinished tasks are completed and that the site is ready for
delivery one business day prior to delivery.
Fail - is issued when less than 80% of the task are completed and all parties cannot agree
that the remaining work will be completed by the requested installation delivery date.
Failed sites will be rescheduled when all items are completed.
2.3.2Quick Installs
Quick installations are described as sites with minimum room improvements required. These
include, but are not limited to the following items:
•Existing electrical disconnect device, wire size and grounds meet all of the above requirements.
•Existing structural items including floor thickness meet all of the above requirements
•Existing HVAC capacity and regulation meet all of the above requirements
•Existing CT suite meets all of the above regulatory and minimum size requirements
•Existing facility can accommodate the delivery and meet all of the above delivery requirements
Quick Installs are subject to the following restrictions:
•Quick installs must have a new room print that accurately reflects the rooms to be upgraded.
•Existing floor anchors from a non-BrightSpeed system CANNOT be reused.
•New floor anchors must be a minimum of 4" from any existing floor penetrations.
Quick Installs typically involve a weekend de-install and room prep completion, with a next business
day delivery and install.
2.3.3"Two-Step" and Upgrade Installs
A "Two-Step" installation is the practice of temporarily installing one CT system in a site with the
intention of upgrading the site to a different CT system at a later date.
•For a "two-step" installation to be considered, the room must meet the minimum room
requirements for the project being upgraded.
•As with any upgrade installation, "two-steps" are subject to ALL of the siting requirements
imposed by the upgrade/final system. This includes the recommended room size as well as
electrical, structural and HVAC requirements.
•Two-steps and other upgrades may be done as "Quick" Installs. In this case, all requirements
described in Section 2.3.2 (above) also apply.
•It is the customer’s responsibility to check that all requirements are met.
•Rooms that do not meet the minimum requirements for the final product must either upgrade
(or enlarge) their room, or consider the "Left-Side Limited Access" option.
Must meet all in section 1 and 2 plus these additions reviewed at the site ready visit.
The GE Healthcare project manager will review the site delivery process with you to determine how
to best transfer the equipment from the transportation truck to your room.
This site ready inspection will review and check these items:
Delivery information
Determine delivery route into the scan room
Determine if tilt dollies or riggers are required
Determine if elevators, doorways and hallways are adequate for delivery
Determine if floor protection is required
Determine if a tilt bed truck is required for ground delivery and ordered.
Regulatory Requirement
Room size meets the minimum requirements
Site print is present and accurately reflects the room size and layout.
No grounded walls are present in the regulatory clearance areas
All regulatory clearances space is met
Room meets all local codes
Manufacturer Requirements: As listed in section 2 - all requirements are met
Purchaser's Site Preparation Work: As listed in section 1 - all actions are completed
Network ID numbers / IP addressesCamera:_________________________________PACS:
____________________________________AW:___________________________________
Other - Specify type & ID:_____________________________________________________________
Other - Specify type & ID:_____________________________________________________________
Camera setup information:_____________________________________________________________
AW Direct Connect address:____________________________________________________________
Do you want HIPAA enabled? No___ Yes ___
Do you want automatic downloads enabled? No___ Yes ___
Table 1-1 Schedule Date Commitments
GECustDates
Y NY N
Has the project schedule been verified with facilities department, contractor, and GE?
Will the committed site-ready date be met?
Does the completion date for any/all construction meet or preceed the delivery date?
Is the Power & Ground survey complete?Date: __________________
Hospital contact: ___________________________________________________
Site-Ready visit is scheduled.Date: __________________
Delivery date is scheduled.Date: __________________
Installation date is scheduled.Date: __________________
Installation timing:A: Weekdays___B: Weekend___C: Quick Install___
If B or C, have all sub-contractors been notified?No___ Yes ___
Does the delivery and/or installation date need to be adjusted?
First-Use date is scheduled.Date: __________________
Must be completed 5 weeks before scheduled delivery dateY NY N
Have final drawings been approved and distributed to the contractors?
Are final drawings “signed off” to approve equipment layout / orientation?
Do the actual room dimensions match those on the final drawings?
Has the radiologist health physician reviewed and approved the room layout and shielding
requirements?
Have any additional requirements or questions about the installation been discussed with GE?
List: ___________________________________________________________
Is there a person assigned to review and verify that all installation requirements are met? Name:
__________________________________________________
Have the specific site requirements been discussed with the contractor?
Refer to the GE final drawings specifications. (See Table 1-3 below.)
Has the responsibility of cabling, installing, and interfacing accessories not on the order been
discussed?
Are all third-party vendors identified, notified and scheduled?
(Examples: Netcom, Medrad, etc.)
Have all regulatory requirements been met per Regulatory Clearances, on page 52?
1 – Intoduction
Will existing network, broadband, and camera cable drops reach new locations and will they meet
the requirements and function with BrightSpeed?
If not, what are the requirements?
List: ___________________________________________________________
Must be completed 5 weeks before scheduled delivery dateY NY N
Has the order been reviewed for completeness and compatibility with existing equipment?
Typical equipment:
Remote monitors ____ AW relocation ____ Cardiac option ____ Injectors ____
Are interfaces to existing and/or new accessories ordered and planned for accordingly?
Have the following peripheral locations been included in the site drawings?
EKG monitor___ Injector control___ Laser camera ___ UPS ___ 2
nd
Monitor___
Will GE Healthcare provide additional services per contract negotiations?
Are correct length cables on order?
Table 1-5 Network Connections
GECustNetwork Installation and Setup
Must be completed 5 weeks before scheduled delivery dateY NY N
Have IP addresses and Host Names been obtained?No___ Yes ___
Will a network camera be used?No___ Yes ___
Mandatory: Is the network installed, are network jacks installed, and is the entire network tested?
Mandatory: Broadband VPN installed/setup?
Mandatory: Are network software options ordered ____ HIS RIS option ___
DICOM print ___ AW ____
Optional: Has modem option ordered? _____ (Requires a site escalation)
Optional: Is the BrightSpeed service telephone line identified and installed for InSite? (Electrical,
mechanical, etc.)
Table 1-6 Miscellaneous Tasks
GECustOther
Must be completed before the scheduled de live ry da teY NY N
Arrangements made in the schedule to allow adequate time for remodeling, if required (such as
wall, floor, or ceiling repair work, painting, other cosmetic finishes)
Have arrangements been made to clean the floor after equipment removal and prior to the
installation of the new equipment?
Is de-installation of existing equipment required? No__
Yes ___ Removal date ___________
Is there a trade-in of existing equipment? No __
Yes __ GoldSeal _____________
Delivery route identified and verified with the proper hospital personnel? No__ Yes __
Elevators and doors checked for size and weight constraints? No__ Yes __
Have appropriate arrangements been made with traffic for delivery?No__ Yes __
This equipment complies with IEC60601-1-2: 2001+A1: 2004 (ED2.1) and IEC 60601-1-2: 2007
(ED3) (if the system rating plate of the scanner marked with IPX0) EMC standard for medical
electrical equipment.
The BrightSpeed System is suitable to be used in the electromagnetic environment, as per the limits
& recommendations described in the tables hereafter:
•Emission Compliance level & limits (see Table 1-7)
•Immunity Compliance level & recommendations to maintain equipment clinical utility (see
Table 1-8, Table 1-9, and Table 1-10).
Note: This system complies with above mentioned EMC standard when used with supplied cables up to
maximum lengths referenced in the MIS MAPS or system cable interconnect diagrams.
4.2Electromagnetic Emission
Table 1-7 Emission Declaration
EMC Emissions Guidance & Declaration for BrightSpeed System
The BrightSpeed System is intended for use in the electromagnetic environment specified
below. The customer or the user of the BrightSpeed System should assure that it is used in such
an environment.
EMC Immunity Guidance & Declaration for BrightSpeed System
The BrightSpeed System is intended for use in the electromagnetic environment specified below.
The customer or the user of the BrightSpeed System should assure that it is used in such an
environment.
Immunity TestIEC 60601-1-2
Test Level
Electrostatic
discharge (ESD)
± 6 kV contact
± 8 kV air
IEC 61000-4-2
Electrical fast
transient/burst
IEC 61000-4-4
± 2 kV for power
supply lines
± 1 kV for input/
output lines
Surge
IEC 61000-4-5
Voltage dips,
short
interruptions and
± 1 kV line-line
± 2 kV line-earth
< 5 % U
T
(> 95% dip in UT)
for 5 sec
voltage
variations on
power supply
input lines
IEC 61000-4-11
Compliance
Level
± 6 kV contact
± 8 kV air
± 2 kV for power
supply lines
± 1 kV for input/
output lines
± 1 kV line-line
± 2 kV line-earth
< 5 % U
T
(> 95% dip in UT)
for 5 sec
Electromagnetic Environment
Guidance
Floors should be wood, concrete, or
ceramic tile. If floors are covered with
synthetic material, the relative
humidity should be at least 30%.
Mains power quality should be that
of typical commercial or hospital
environment.
Mains power quality should be that
of a typical commercial or hospital
environment.
Mains power quality should be that
of a typical commercial or hospital
environment. If the user of the
BrightSpeed System requires
continued operation during power
mains interruptions, it is
recommended that the BrightSpeed
System be powered from an
uninterruptible power supply or a
battery.
Power frequency
3 A/m3 A/mPower frequency magnetic fields
(50/60 Hz)
magnetic field
IEC 61000-4-8
Note : U
is the a.c. mains voltage prior to application of the test level.
T
Page 38 Chapter 1 - Introduction
should be at levels characteristic of a
typical location in a typical
commercial or hospital environment.
The System is intended for use in the electromagnetic environment specified below. The
customer or the user of the System should assure that it is used in such an environment.
Immunity TestIEC
60601-1-2
Test
Level
Conducted RF
IEC 61000-4-6
3
VRMS
150kHz to
80 MHz
Radiated RF
IEC 61000-4-3
(alternative
3 V/m
80 MHz to
2.5 GHz
method: IEC
61000-4-21)
Complian
ce Level
3 V
150kHz to
80 MHz
3 V/m
80 MHz to
2.5 GHz
Electromagnetic Environment Guidance
Portable and mobile RF communications
equipment should be used no closer to any part of
the System, including cables, than the
recommended separation distance calculated from
the equation appropriate for the frequency of the
transmitter.
Recommended Separation Distance
(see Table 1-10)
80 MHz to 800 MHz (see Table 1-10)
800 MHz to 2.5GHz (see Table 1-10)
where P is the maximum output power rating of the
transmitter in watts (W) according to the transmitter
manufacturer and d is the recommended separation
distance in metres (m).
Field strengths from fixed RF transmitters, as
determined by an electromagnetic site survey
a
,
should be less than the compliance level in each
frequency range
b
.
Interference may occur in the vicinity of equipment
marked with the following symbol:
1 – Intoduction
a
Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless)
telephones and land mobile radios, amateur radio, AM and FM radio broadcast, and TV
broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic
environment due to fixed RF transmitters, and electromagnetic site survey should be
considered. If the measured field strength in the location in which the System is used exceeds
the applicable RF compliance level above, the System should be observed to verify normal
operation. If abnormal performance is observed, additional measures may be necessary, such
as re-orienting or relocation the System.
b Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
Note : These guidelines may not apply in all situations. Electromagnetic propagation is affected
by absorption and reflection from structures, objects, and people.
Recommended separation distances between portable and mobile RF communications
equipment and the BrightSpeed System.
The BrightSpeed System is intended for use in an electromagnetic environment in which radiated
RF disturbances are controlled. The customer or the user of the BrightSpeed System can help
prevent electromagnetic interference by maintaining a minimum distance between portable and
mobile RF communications equipment (transmitters) and the BrightSpeed System as
recommended below, according to the maximum output power of the communications
equipment.
Separation distance according to frequency of transmitter
150 kHz to 80 MHz
80 MHz to 800MHz
800 MHz to 2.5 GHz
Rated Maximum Output
Power (P) of Transmitter
Watts (W)
Separation
Distance meters
Separation
Distance meters
Separation
Distance meters
0.010.120.120.23
0.10.370.370.74
11.171.172.33
103.693.697.38
10011.711.723.3
For transmitters rated at a maximum output power not listed above, the separation distance can
be estimated using the equation in the corresponding column, where P is the maximum output
power rating of the transmitter in watts (W) according to the transmitter manufacturer.
Note 1: At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
Note 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected
by absorption and reflection from structures, objects, and people.
4.3.1Limitations Management :
Adhering to the distance separation recommended in Table 1-10, between 150kHz & 2.5GHz, will
reduce disturbances recorded at the image level but may not eliminate all disturbances. However,
when installed and operated as specified herein, the system will maintain its essential performance
by continuing to acquire, display, and store diagnostic quality images safely.
(*) For example, a 1W mobile phone (800MHz to 2.5GHz carrier frequency) shall be put 2.3 meters
apart from the BrightSpeed System (in order to avoid image interference risks).
4.4Use Limitation :
4.4.1External components
The use of accessories, transducers, and cables other than those specified may result in degraded
ELECTROMATHNETIC COMPATIBILITY of the BrightSpeed System .
4.5Installation Requirements & Environment Control :
In order to minimize interference risks, the following requirements shall apply.
4.5.1Cable Shielding & Grounding
All interconnect cables to peripheral devices must be shielded and properly grounded. Use of
cables not properly shielded and grounded may result in the equipment causing radio frequency
interference.
4.5.2This product complies the radiated emission as per CISPR11 Group 1 Class A
standard limits
The BrightSpeed System is predominantly intended for use, in non-domestic environments, and not
directly connected to the Public Mains Network. The BrightSpeed System is predominantly intended
for use (e.g. in hospitals) with a dedicated supply system, and with a X-ray shielded room. In case
of using in a domestic environment (e.g. doctor’s offices), in order to avoid interferences, it is
recommended to use a separated AC power distribution panel & line with a X-ray shielded room.
4.5.3Subsystem & Accessories Power Supply Distribution
All components, accessories subsystems, systems which are electrically connected to the
BrightSpeed System, must have all AC power supplied by the same power distribution panel & line.
4.5.4Stacked Components & Equipment
The BrightSpeed System should not be used adjacent to or stacked with other equipment; if
adjacent or stacked use is necessary, the BrightSpeed System should be observed in order to verify
normal operation in the configuration in which it will be used.
4.5.5Low Frequency Magnetic Field
In case of a digital BrightSpeed System, the Gantry (digital detector) shall be apart 1meter from the
generator cabinet, and 1meter apart from the analog (CRT) monitors. These distance specifications
will minimize the low frequency magnetic field interference risk.
4.5.6Static Magnetic Field Limits
In order to avoid interference on the BrightSpeed system, static field limits from the surrounding
environment are specified.
Static field is specified less than <1 Gauss in Examination room, and in the Control Area.
In order to reduce electrostatic discharge interference, install a charge dissipative floor material to
avoid electrostatic charge buildup.
The relative humidity shall be at least 30 percent.
The dissipative material shall be connected to the system ground reference, if applicable.
Before a BrightSpeed system can be installed, all pre-installation requirements must be complete.
•Chapter 4, Sections 8.0 and 9.0
Structural Requirements
•Chapter 4, Section 10.0
Radiation Protection
•Broadband standard•Chapter 9, Interconnection Data
•Site Ready Visit
Site-specific items must be verified before the installation can begin.
Section 1.0
Dust/Dirt Contamination
The BrightSpeed systems (consisting of: Console, PDU, Table and Gantry) are highly susceptible
to airborne contaminants, especially concrete and drywall dust. Due to the possibility of
contamination, these systems should NEVER be installed in a construction site.
•Chapter 8, Power Requirements
(Site Power Audit Required)
2 – Overview
NOTICE Any site with unfinished floors, walls or ceilings is considered a construction site, and is not
suitable for system installation.
Section 2.0
Chemical Contamination
Wet film processors must never be installed in the same room as the scanner, due to the possibility
of chemical contamination of BrightSpeed Series components. Such chemicals can contribute to
increased equipment failures, increased system downtime, and decreased reliability. Film
processor equipment installation must meet the manufacturer’s requirements (e.g. ventilation
specifications) and all applicable national and local codes. Also, consideration’s should be given to
the location of this equipment and chemical fumes relative to human contact as it relates to locating
this equipment and chemicals in the control room.
Section 3.0
Walls, Ceiling and Floor
All walls, ceiling, and flooring must be completed before installation can begin.
For structural requirement, refer to Chapter 4, Section 8.0, on page 84.
For information on Broad-band requirements, refer to Chapter 4, Section 9.0, on page 87.
Section 5.0
Phone Line (for optional modem)
Two phone lines must be installed at or near the console and be operational prior to installation.
•1-Analog line (for modem use)
•1-Voice line
Section 6.0
Review
The BrightSpeed Series systems use adjustable leveling pads to support the gantry and table. The
gantry has four (4) primary leveling pads. The table has five (5) pads used for leveling it.
Using the GE print to establish the room layout, make sure all the operating and service clearances
shown on the print are observed. Using the template (P/N 5160024/5341997) shipped with the
system, locate the anchor holes. Make sure they clear structural interferences in the floor.
Clean the area. Free the mounting surface of any material that may interfere with the positioning
and leveling of the system.
1.)Lay out the 2 floor templates.
2.)Start with the Gantry template—align per the GE print.
3.)Place the table template over the top of the Gantry template. Align the scan and table centerlines and secure the templates to the floor. Make sure there are no potential clearance issues.
4.)Check the level of the floor (See Figure 2-1) across the templates. This should be measured
on the template over the table/gantry area, as shown in Figure 2-1 below.
FLOOR LEVELNESS SPECIFICATION: 6 mm (1/4 in.) over 3 m (10 ft.)
Note: Tiles (or other resilient flooring) around all holes will be cut during the installation process.
The following is a list of system options requiring site planning work for the BrightSpeed system.
Contact your local GE Medical Systems Sales representative for a complete list of all system
options or visit us at www.gehealtcare.com. Refer to the instruction manuals supplied with specific
options for respective details.
CATALOG NUMBEROPTION DESCRIPTION
B7850LD/B78502LDInternational Dolly Set
B79302CASingle-piece desktop kit
B79312CASide-by-side desktop kit (Freedom WorkSpace)
B78442CA* Freedom Workspace Standard
B78452CA*Freedom Workspace kit Wide
B7866ABSmartScore Option, EKG Monitor and Recording Device
B7900WB* SmartScore 4.0 Package
B7500PLConnectPro Option (SW & Bar Code Reader), provides
B7500LN* ConnectPro HIS/RIS SW Key (LINUX) Hospital Info
B7540RBBar Code Reader
B7877BC* Bar Code Reader (USB)
B7710LNBoom in a Room monitor
B71182CALong Cable Set
B71172CAShort Cable Set
B7700MGGlobal Modem Kit
B77302CABSD Global USB Modem
B7850TCRear Cable Cover Assembly
B7700SBLimited Access Option
B75792CA/ B75022BSGantry Accessory I/F HW
B75802CAAC Outlet Box for OC
B75822CA/ B75002BEXtream Injector
B75832CA/ B75012BEEnhanced Xtream Injector
B78462CA*Recon Enhancement
E6315JE*DIACOR CARBON OVERLAY VCT
B75812CA16FPS Upgrade
Minimum Width: 3353 mm (11ft. ); 356 mm (14in. ) cover to wall
Average Width: 3708 mm (12ft. 2in. ); 711 mm (28in.) cover to wall
Short Footprint (length only):
Minimum length: 5480 mm (18ft. )
Additional component dimensions are available in Figure 4-7 through Figure 4-15 of this document.
Consult your local General Electric Project Manager of Installation for your appropriate room
specifications.
For equipment clearance requirements, refer to Section 2.0. Remember, sufficient Regulatory and
Service clearances must be maintained around equipment for full operation, service and safety.
Cable length is an important consideration in room layout. A set of short cables (B71172CA) and a
set of long cables (B71182CA) are optional for BrightSpeed system.
Note, also, that where possible, the cables should enter the gantry from the rear, utilizing the rear
cable cover assembly. Alternate cable entry is possible at the center of the gantry (refer to the
Installation template).
•Excess cable length cannot be stored behind the console or PDU.
•Long cable must not be cut or shortened.
•Excess cable may be stored in conduits, a cable storage box if present, or the floor duct,
provided sufficient space is available. Observe the fill rate for each option. If there are
questions regarding local electrical or building codes, consult the project electrical contractor
or electrician.
•All NEC 70-E Electrical Regulations regarding conduit or duct fill must be observed.
4 – Room Planning
Chapter 4 - Room PlanningPage 51
Page 52
GE HEALTHCARE
914 to 1219mm
(36 to 48 in.)
914 to 1219mm
(36 to 48 in.)
Ta b l e
Super
Structure
Footprint
Gantry Super
Structure
Footprint
Table
Base
Cradle
&
Extender
Foot
Switch
Asm
3212mm (10ft. 6in.)
1861mm (6ft. 1in. )
36"
2
8
“
36"
3
6
"
2057 mm
( 6ft. 9in. )
Regulatory Compliance
Workspace Clearance
Perpendicular to Equipment
Regulatory Compliance 711 mm
28 inch Egress Clearance
Reference Regulatory Clearance Tables
on following pages
for minimum and variable distance definitions
and additional metric conversions.
2
8
“
A
C
B
A) Minimum Room
(Less than 711 mm (28 in. ))
B) Minimum Room
(Less than 914 mm (36 in. ))
C) Recommended Room
(914 mm (36 in.) or Greater)
MINIMUM CLEARANCES UNDER U.S. FEDERAL REGULATIONS AND NATIONAL
STANDARDS: 29 CFR 1910 (OSHA), NFPA 70E (STANDARD FOR ELECTRICAL
SAFETY IN THE WORKPLACE), AND NFPA 101 (LIFE SAFETY CODE):
Figure 4-1 is a map of clearance requirements for U.S. regulatory compliance. See clearance tables
on the following pages for detailed dimensional clearances. Please note all systems installed in the
United States must comply with all Federal and local regulations. For installations outside the
United States, country-specific or other local regulatory clearance requirements must be met.
Figure 4-1 Regulatory Clearance Requirements for BrightSpeed System Configurations
Egress: 29 CFR 1910 Subpart E (OSHA) and NFPA 101 (Life Safety Code) define the minimum
requirements for means of egress. The requirement most applicable to equipment installation and
room layout is minimum width of exit access. Under OSHA 1910.37(f)(6), the minimum width of exit
access shall in no case be less than 28 in. from any potentially occupied point in the room.
Under NFPA 101 (2006 edition) 7.3.4.1, the minimum width of any means of egress is 36 in.
However, NFPA allows this to be reduced to 28 in. around furniture or equipment, provided that a
36 in. clearance would otherwise be available without moving permanent walls.
Electrical Clearance: 29 CFR 1910 Subpart S (OSHA) and NFPA 70E (Standard for Electrical
Safety in the Workplace) define minimum clearance requirements for the workspace around
electrical equipment. Under both OSHA 1910.303(g)(1) and NFPA 70E (2004 edition) 400.15, a
minimum clear space of 36 in. depth (with minimum 30 in. width and 78 in. height) must be provided
in front of electrical equipment with parts operating at 600 volts or below and likely to require
examination, adjustment, servicing, or maintenance while energized.
This safety clearance requirement applies to all GEHC equipment. Although 36 in. is the minimum
clearance for most installations, the standards require an increased minimum clearance distance
where parts operate above 150 volts (but still below 600 volts) under the following circumstances:
•If the wall or surface directly facing the electrical equipment is grounded (e.g. brick, concrete,
or tile) or includes grounded protrusions (such as medical gas ports, metal door or window
frames, water sources and metallic sink structures, metallic cabinetry, electrical disconnects or
emergency off panels, air conditioners or vents), then a 42 in. clearance depth is required.
If the possibility exists of exposed and unguarded live parts on both sides of the workspace (for
example if a power distribution unit were positioned on the wall directly facing the GEHC
equipment), then a 48 in. clearance depth is required.
2.1.2Regulated Minimum Working Clearance by Major Subsystem
Requirements apply to equipment operating at 600V or less, where examination, adjustment,
servicing, or maintenance is likely to be performed while live parts are exposed.
Direction of Service Access is defined as perpendicular to the surface of the equipment being
serviced.
•Required regulatory clearance distances must be maintained and may not be used for storage.
This includes normal system operation as well as service inspection or maintenance..
Work Space
Requirement
Direction of Service
Access: front of console
Service access width:
Front of console
Table 4-3 Console Subsystem
Minimum Clear
Space
914 mm (36 in.)There are no exposed live part hazards with
762 mm (30 in.)This is the width of the workspace in front of
Additional Conditions
the cover in place. If the console is placed
under a counter, the front edge of the
console must be even with the vertical edge
of the console workspace.
Note: This component is typically serviced
from the front with access to the rear.
the equipment. A minimum of 762 mm (30
in.) or the width of the equipment, whichever
is greater, is required.
762 mm (30 in.)This is the width of the working space in
(Left-Right of workspace)
Table 4-5 Gantry Subsystem
Work Space
Requirement
Direction of Service
Minimum Clear
Space
914 mm (36 in.)There are no exposed live parts hazards
Access (Table Head or
Foot)
Direction of Service
914 mm (36 in.)**This distance can be reduced to 711 mm
Access (Table Sides)
Direction of Service
711 mm (28 in.)For the front gantry cover removal, a
Access (Table Foot)
Service Access Width
762 mm (30 in.)This is the width of the working space in
(Left-Right of workspace)
Additional Conditions
front of the equipment. A minimum of 762
mm (30 in.) or the width of the equipment,
whichever is greater, is required.
Additional Conditions
with the cover in place.
This component is typically serviced form all
four sides.
this is the width of the workspace on each
side of the equipment. A minimum of 914.4
mm (36 in.), or the width of the equipment,
whichever is greater, is required.
(28 in.) provided a written and signed
approval is obtained by the local team from
the local AHJ (Authority Having
Jurisdiction). The signed document must be
on file with GE.
minimum of 457 mm (18 in.) is allowed only
if an unobstructed egress space of 711 mm
(28 in.) is maintained around the equipment
for room exit. This also means no trip
hazards exist along the path of egress.
front of the equipment. A minimum of 762
mm (30 in.) or the width of the equipment,
whichever is greater, is required.
914.4 mm (36 in.)* There are no exposed live part hazards with
the cover in place.
This component is typically serviced from
the front with access to the rear.
*If exposed live parts of 151 - 600 volts are
present, 1219 mm (48 in.) is required on
both sides of the workspace with the operator between.
*If the opposite wall is grounded and
exposed live parts of 151 - 600 volts are
present, 1067 mm (42 in.) is required.
Service Access Width
(Right side and length of
UPS)
762 mm (30 in.)This is the width of the working space in
front of the equipment. A minimum of 762
mm (30 in.) or the width of the equipment,
whichever is greater, is required.
Head Clearance1981 mm (78 in.)This is the height of the workspace
measured from the floor at the front edge of
the equipment to the ceiling or overhead
obstruction(s). A minimum of 1981 mm
(78 in.) or the height of the equipment,
whichever is greater, is required.
Table 4-7 UPS Subsystem
Work Space
Requirement
Direction of Service
Access (Front of A1
Disconnect)
Minimum Clear
Additional Conditions
Space
914.4 mm (36 in.)* There are no exposed live part hazards with
the cover in place.
This component is typically serviced from
the front with access to the rear.
*If exposed live parts of 151 - 600 volts are
present, 1219 mm (48 in.) is required on
both sides of the workspace with the operator between.
*If the opposite wall is grounded and
exposed live parts of 151 - 600 volts are
present, 1067 mm (42 in.) is required.
Service Access Width
(Right side and length
of A1 Disconnect)
762 mm (30 in.)This is the width of the working space in
front of the equipment. A minimum of 762
mm (30 in.) or the width of the equipment,
whichever is greater, is required.
Head Clearance1981 mm (78 in.)This is the height of the workspace
measured from the floor at the front edge of
the equipment to the ceiling or overhead
obstruction(s). A minimum of 1981 mm
(78 in.) or the height of the equipment,
whichever is greater, is required.
Egress: The path of exit from within any room. U.S. regulations require a minimum of 711.2 mm (28
in.) of continuous and unobstructed space, including trip hazards along the path of exit.
Workspace: The dimensional box required for safe inspection or service of energized equipment.
It consists of depth, width, and height. The depth dimension is measured perpendicular to the
direction of access. The U.S. regulation minimum is 914.4 mm (36 in.), but additional conditions can
increase the minimum dimension requirement. GEHC defines this as the envelope of the
component superstructure with the external covers in place.
Service Access Width: The width of the workspace in front of the equipment. A minimum of 762
mm (30 in.), or the width of the equipment, whichever is greater.
Head Clearance: The height dimension of the workspace. The height of the workspace measured
from the floor at the front edge of the equipment to the ceiling or overhead obstruction(s). 1981.2
mm (78 in.), or the height of the equipment, whichever is greater.
Grounded Wall: Any wall that can be electrically conductive to earth ground. Masonry, concrete,
and tile are considered conductive. Additional commonly found aspects of a wall should also be
considered grounded. This is not an all-inclusive list:
•Medical gas ports and plates
•Metal doors and window frames
•Water sources and metallic sink structures
•Metallic wall-mounted cabinetry
•A1 main disconnect panel
•Equipment Emergency Off panels
•Industrial equipment (such as air conditioners and vents)
•Expansion joints
•Surface raceway
•Exposed wall conduits
•Floor outlets boxes
The following are not considered as grounded elements of a common wall:
The CT Gantry Left Side Limited Access Initiative provides the capability to reduce the minimum
room size for CT Systems while still meeting all installation requirements and specifications. This
adds left side flexibility, allowing the CT system to be sited in rooms with widths 559 mm (22 in.)
smaller than the current minimum room width. Left-side access and egress may be restricted. Refer
to your site's installation print for your room's detail.
If you are using the square meters (square feet) to determine compliance, remember that the front
cover clearance is wider than the regulatory clearance along the table length, and that the cover
park position is behind the table in the home position. The cover is removed on tilting dollies and
can be moved side-to-side to reach the park position of 457 mm (18 in.), if this is not an egress
route.
Wall duct and conduit on walls within the regulatory clearance areas shall be 1067mm (42 in.),
measured from the covers to the obstruction. Servicing of the CT System can be safely performed
within the regulatory envelopes, however sufficient space must be maintained to remove system
covers, and replace large system components. To achieve this clearance for the gantry, clear
space must be available to maneuver the gantry covers mounted on the service dollies. Surface
floor raceway cannot be used in the egress route areas. OSHA ramps are available. The FE lifting
the rear or front cover to avoid floor obstructions is not an EHS-approved service procedure. One
Service Engineer shall be able to accomplish all service component replace tasks listed without
the need for special tools or equipment, such as a tube change, detector change, and HV tank.
2.2.1.1Regulatory Caution
Site prints are required for all system installations including relocation and moves. CT room layout,
as shown on your site print, shall meet all regulatory requirements as described in the installation
manual. Additional room components, such as cabinets, reduce room size. Equipment not shown
on the site print may void the caution statement, making the room non-compliant. Actual site
measurements before installation will be taken to determine room size and compliance.
2.2.1.2Egress Clearance
Egress requires a clear, unobstructed route out of the room, either around the back of the gantry or
around the back of the table. If your egress route is not around the back of the table, maintain 457
mm (18 in.) of clearance between the back of the table, with a continuous width of 3200 mm (126
in.), 1600 mm (63 in.) on each side of the table center line, on each side to any obstruction so that
the front cover can be removed. Refer to the Pre-Installation manual for more details on service
clearances.
Exceptions
Rooms smaller than 3353 mm x 6096 mm (11 ft. x 20 ft. ), require construction to meet the minimum
requirements. The design center or your GE PMI may have additional recommendations for your
room size.
2.2.1.3Operational Caution
In a minimum room layout 356 mm - 686 mm (14 in. - 27 in.), the customer should consider
workflow, customer access for patient care, and critical-care operations space requirements.
Additionally, there may be limited equipment access on the gantry left side when loading patients
or when positioning patient equipment in the room between the gantry and the wall. Detailed
customer installation tasks are detailed in the product Pre-Installation manual, Chapters 1-4.
This room configuration offers the most flexibility for future upgrades. It has sufficient workspace
and space to add millwork, while meeting all regulatory requirements. This room would be
compatible with most two-step future installations.
Recommended Room Size
3962 x 6299 mm (13ft. x 20ft. 8in. )
Same Regulatory requirements apply
2.2.2.2Typical Room Size
This room size and configuration is commonly found on most sites and allows for some future
upgrades. It has sufficient workspace but limited space to add millwork and meet all regulatory
requirements. This room may be compatible with some two-step future installations.
Typical Room Size
3912 x 5868 mm (12ft. 10in. x 19ft. 3in. )
Same Regulatory requirements apply
2.2.2.3Minimum Room Size
This room size and configuration is the smallest functionally acceptable space for this product. Size
and layout often eliminate these rooms for future upgrade considerations. Due to limited size,
equipment and regulatory requirements, this room often has limited workspace, and very limited or
no in-room millwork, but still meets all regulatory requirements. This room is not compatible with
two-step future installations
If you are using the square footage (Sq M) to determine compliance, remember that the front and
rear cover clearances are wider than the regulatory clearance along the table length, and that the
cover park position is be hind the table in the home position. The rear cover is also on wheels and
must be able to be removed from behind the gantry for service.
Minimum Room Size
3353 x 6096 mm (11ft. x 20ft. )
Same Regulatory requirements apply, with the addition of no energized left side service.
4 – Room Planning
Chapter 4 - Room PlanningPage 59
Page 60
GE HEALTHCARE
How to measure
From the farthest outward component
No obstruction areas
Gantry
Side vertical covers outward
Front or back vertical covers outward
Not from the base covers
Table
Table cradle covers outward
Back of cradle outward
Room B - Less than 36 in. but greater than 28 in. measured from the covers to the left sidewall.In
this configuration service, egress and workspace are acceptable around the gantry.
Servicing of the CT System can be safely performed within the regulatory envelopes defined in
Section 2.1 , however sufficient space must be maintained to remove the covers from the system.
To achieve this clearance for the gantry, clear space must be available to maneuver the gantry
covers mounted on the service dollies. One Service Engineer can accomplish this.
•Gantry front cover removal requires the use of the “Tilting Cover Dollies”. These dollies allow
the Service Engineer to separate the cover from the gantry, tilt the cover 90 degrees, roll the
cover to the foot end of the table, and then tilt the cover an additional 90 degrees such that the
front cover is now upside down relative to the normal system mounted condition.
illustrates the minimum clear space required to achieve this operation. The gantry front cover
must be removed to a position that satisfies the minimum regulatory clearances.
•The gantry rear cover, with service dollies installed, requires a width 2244 mm (88 in. ) and a
depth of 610 mm (24 in. ) of clearance for removal. Sufficient space must be calculated to move
the cover either straight back or to a side of the table to satisfy the minimum regulatory
clearance shown in
rear or either side of the gantry.
•If gantry service requires both the front and rear covers be removed, then these covers must
be positioned within the room in such a manner as to not violate the regulatory clearances on
any side of the gantry. This may necessitate removing the covers from within the suite. This
should be discussed with the customer and provisions made to accommodate this potential
event.
•A single Service Engineer can safely perform servicing of the table. Sufficient clear space must
be available to maintain regulatory clearances when the table covers or cradle are removed.
•In your room layout design, service shall have clear and unobstructed access to the gantry
tube change area for all major component replacements. These components must be able to
reach the service area without lifting or rigging by one service engineer. Major components
include:
-CT X-ray tube in crate
-High voltage tank(s) in crate
-Slipring in crate
-Detector assembly
Be aware of cabinet placement, and how surface floor ducts are used in room configurations.
Figure 4-2. This means the rear cover cannot violate the workspace on the
Figure 4-2
3.2Gantry Service Clearance
4 – Room Planning
Specifications for Boom Assembly clearance arc are defined in . The boom assembly is used during
tube and detector replacement. The minimum ceiling height within the clearance radius is 2286 mm
(90 in.).
3.3Power Distribution Unit (NGPDU) Service Clearance
Positioning of this component must be considered for regulatory compliance as defined in
Section 2.1 , Regulated Minimum Working Clearance by Major Subsystem.
See Regulatory Tables.
3.4Console Service Clearance
The console does not present an exposed live parts hazard. However, a minimum working space
depth of 1219.2 mm (48 in.) and full width of the console be maintained at all times for service
activity. Additionally sufficient space needs to be provided for repositioning of the console and side
clearance for rear service access. Egress as well as other service requirement shall be considered
when siting the console. See Figure 4-6 for a Recommended control room layout.
Section 4.0
Short Footprint Consideration
4.1Introduction of Short Footprint function
If the site room length cannot satisfy the requirements for standard mode. Short Footprint mode can
be considered.
Short Footprint mode is to set limitation to table cradle scannable limitation(A) so that cradle cannot
move in out of the limitation. The scannable range is limited accordingly.
Short Footprint features are as follows:
Page 66 Section 4.0 - Short Footprint Consideration
•Cradle Movement limitation can be set at any position.
•Table Height Limitation can not be set (no change for footprint at Gantry Front side).
•Scannable range is depends on the Gantry Rear space (distance to the wall), but need to
consider the Service Clearance and country's local regulation for Gantry Rear space.
4.2Instruction of using Short Footprint function
NOTICE Cradle limitation must comply with country or local regulatory clearance requirements.
Cradle movement limitation set for short footprint must be approved by customer during preinstallation.
1.)Refer to Figure 4-4 , use floor template with ruler to prearrange the layout and calculate the
cradle scannable limitation (A).
2.)Make GE siting print to meet regulatory and service clearance requirements.
3.)Record the distance from cradle limitation to wall (X) and cradle scannable limitation (A) for
installation.
A: Cradle Scannable Limitation, the value to be set using Short Footprint function
A(Scannable Range(approx.)) = 643mm(Scan Center Line to Gantry Rear Cover)
+ B(Gantry Rear Cover to Wall) - X(Safety Clearance to prevent hitting cradle to wall).
B: Gantry rear cover to wall, no less than 914 mm (36 in.)
Note: When the length from Gantry rear cover to wall is 914mm, cradle scannable limitation would be
1457mm (Shown in Figure 4-5).
D: Gantry left side to wall, no less than 356mm (14 in. ). Refer to Section 3.0 for details about
Limited Access.
E: Gantry right side to wall, no less than 914 mm (36 in. ). If Short Footprint is set for a short room
length, bigger gantry side clearance is required to remove Gantry rear cover, or no removal of rear
cover is accepted.
X: Distance from cradle limitation to wall.
NOTICE It is Suggested that safety clearance from cradle IN-limit to wall should be no less than 100 mm.
Figure 4-5 shows minimum room layout with Short Footprint function (Gantry rear cover can be
removed).
Figure 4-5 Minimum Room layout for Short Footprint function
Page 68 Section 4.0 - Short Footprint Consideration
Two kinds of Console configurations are available:
•Standard Console: Console + Single Piece Desktop;
•Console with FWS: Console + Freedom Workspace Table (See Figure 4-6).
Console
AW
Figure 4-6 Recommended Control Room Layout with Freedom Workspace (FWS)
NOTICE If a Freedom Workspace (FWS) console table is ordered, it MUST be placed side by side with the
console. It can be placed on either side of the console. The Extended Cables Kit is shipped in FWS
Console Table Assembly. The extended cable length is 3 m (see Chapter 9 Section 3.2 for details).
FWS
2500 mm (8ft. 2in. )
3861 mm (12ft. 8in. )
4 – Room Planning
•The control room must provide a suitable operating environment for the console electronic, and
operator working comfort.
•The console cannot be dismantled of, have components removed or rearranged in
configurations other than as shipped.
•If operationally possible, the monitor desktop and user desktop components may be removed
and placed on a counter-top, providing the cable lengths shipped are not altered or changed.
The operator console cabinet then can be remote mounted, provided the cooling requirements
are met. Maintain 152mm (6 in. ) on all sides; and venting is required.
•A suitable work area, which is within reach of the operator's console, should be provided for
placement of the injector control. Injector controls differ in dimensions depending on the brand
selected.
•A PACS, workstation, image printer, or filming device are often placed in the operator console
control room area, and sometimes may be directly linked to the operator console.
•Additional components although linked via network or ethernet cable, are not powered from
the CT operator console.
•Additional room power and network connection should be considered when reviewing the
console work space.
5.2Storage Cabinet
A storage cabinet is provided by GE Healthcare to store all supplied service equipment (see
Table 4-9 for equipment list). This storage cabinet (457 mm D x 914 mm W x 1067 mm H) (18 in.
D x 36in. W x 42in. H; ~90 lbs) should be located in the scan room suite area, for easy service
access. A storage Cabinet is provided as option (B77292CA)
ITEMSIZEWEIGHT (TOTAL)
QA Phantom (water filled)20 x 15 cm
(7.9 in. x 5.9 in. )
35CM Phantom35 x 7 cm
(13.8 in. x 2.8 in. )
48CM Phantom48 x 7 cm
(18.9 in. x 2.8 in.)
Phantom Holder25 x 25 cm
(9.8 in. x 9.8 in.)
FE Box30 x 38 x 30 cm
(11.8 in. x 15 in. x 11.8 in.)
Rear Cover Dollies158 x 82 cm
(62.2 in. x 32.3 in.)
Front Cover Dollies85 x 20 cm and 85 x 15 cm
(33.5 in. x 7.9 in. and 33.5 in. x
5.9 in.)
Install Support Kit (box)30 x 30 x 38 cm
(11.8 in. x 11.8 in. x 15 in.)
Tube Hoist Kit77 x 8 cm and 38 x 15 cm
(30.3 in. x 3.1 in. and 15 in. x
5.9 in.)
Balance Weight Kit33 kg73 lb
Table 4-9 Equipment to be stored in storage cabinet
5.5 kg12 lb
8.2 kg18 lb
11.4 kg
3.6 kg8 lb
6.8 kg15 lb
11.4 kg25 lb
15.9 kg35 lb
9.1 kg20 lb
9.1 kg20 lb
25 lb
5.3Advantage Workstation (AW)
Refer to Advantage Workstation Pre-Installation Manual and Installation/Service Manual.
Ceiling Pedestal mount lowest point to floor (Injector or Monitor) 2134.0 mm (84.0 in)
7.2System Operation
SYSTEM OPERATION MMINCHES
Finished ceiling to floor (recommended) 2743.0mm108.0 in.
Finished ceiling to floor (minimum) 2286.0mm 90.0 in.
HPower Table max extension head end w/extender from Center Line2030.0mm 80.0 in.
HPower Table extension head end w/extender to obstruction 152.0mm 6.0 in.
HPower Table in lowest pos. w/cradle @home pos. to Center Line3209.0mm126.5 in.
GT1700 Table max extension head end w/extender from Center Line 1712.0 mm 67.0 in.
GT1700 Table extension head end w/extender to obstruction 150.0 mm 6.0 in.
GT1700 Table in lowest pos. w/cradle @home pos. to Center Line 3209.0 mm 126.5 in.
GT1700 Table in lowest pos. w/cradle @home pos. to surface of Gantry front cover 2744.0 mm 108.0 in.
Back of GOC4/LCGOC/AIO Console to wall152.0mm6.0 in.
Back of TIO/NIO16 Console to wall96.0mm4.0 in.
Back of PDU to wall 152.0mm 6.0 in.
7.3Injector Control
A suitable work area, which is within reach of the operator's console, should be provided for
placement of the injector control.
Wall mounted, ceiling mounted and pedestal units need cables to be routed from the gantry area to
the console area. Injectors AC power is supplied with Accessory I/F hardware kit.
Note: Injector cables should not be routed with the system cables.
Mounts are available in different configurations and lengths. Refer to Injector documentation for
detailed installation instructions.
IMPROPERLY SECURED TABLE MAY TIP, DISLODGING PATIENT.
PROPER ANCHORING IS KEY TO MAINTAINING PATIENT SAFETY DURING
SYSTEM OPERATION.
NOTICE It is the purchaser's responsibility to provide an approved support structure and mounting
method for all floor types other than those listed. General Electric is not responsible for any
failure of the support structure or method of anchoring, including seismic requirements.
GE is not responsible for methods other than those listed.
Table and gantry mounting dimensions are shown in Figure 6-2, Figure 6-3, Figure 6-4, and
Figure 6-5. Refer to Chapter 6 for additional details of floor loadings, component weights, and
Gantry and Table installation and anchoring.
Anchor gantry and table to floor by a means that will maintain their relative alignment and meet
applicable building and other local codes, including seismic structural mounting requirements.
Floor structure must be capable of withstanding the occupied weight of table and gantry, and the
individual contact area loading of these components. Refer to Section 6.0 for each of the three (3)
major components of the BrightSpeed system.
Support areas of the patient table and gantry must rest on solid concrete, not resilient tile or
carpeting which will slowly yield over a period of time and disturb alignment of table to gantry.
Factors that could cause misalignment between gantry and table due to floor sag should be
considered. The cradle can potentially carry a 205 kg (450 lb) (HPower Table) / 227 kg (500
lb) (GT1700 Table) patient. Center of gravity changes as cradle cantilevers.
Take into consideration all other moving weights such as gurneys or personal equipment. Refer to
Chapter 6 for gantry and table mounting details.
No part of floor surface within table and gantry, nor the two interface areas between table and
gantry, should be higher than the support area for table and gantry.
8.2Floor Anchors
Provided floor anchors are designed for use ONLY on concrete floors that meet the 102 mm (4 in.)
concrete floor requirements. All other anchoring methods (on floor types other than the 102 mm (4
in.) concrete minimum) must be determined to meet the stated GE minimum load requirements, at
the customer’s expense, by their structural contractor. The customer’s contractor is responsible for
the installation of all anchors other than those shipped with the system.
Concrete floors must have a minimum strength of f'c = 2000 psi (1.4 X 107 Pa) at 28 days (curing
time) for mounting floor anchors. It is the responsibility of each customer to have appropriate tests
performed to determine and measure concrete strength.
Note: If installing the GE BS scanner on a floor type thinner than a 102 mm (4 in. ) concrete floor, the
purchaser, at their expense, shall provide acceptable anchoring and mounting methods that meet
all structural specifications provided in sections 8.1 through 8.5 of this Pre-Installation Manual.
8.4Floor Levelness
The CT Room floor levelness requirement is important for accurate patient positioning. Floor
levelness in the Scan Room must not be greater than 6 mm (0.25 in. ) between depression and high
spots over any 3048 mm (120 in. ) distance within the area of the gantry/table template (see
Figure 2-1, on page 45).
Note: Floor must meet levelness specification to properly align the table gantry. Minimum gantry height at
this specification will be 1/2" (15 mm) to prevent cable crushing.
Table level may not be achievable if overall floor levelness is greater than the specification.
Overall floor level must be 0" to use under gantry cable entrance. Minimum gantry height will be
3/4" 20 mm with this option to prevent cable crushing.
The use of floor shims is not suitable to achieve floor levelness. It is recommended that the concrete
be leveled to meet this requirement.
8.5Floor Vibration
The CT equipment may be sensitive to vibration in the frequency range of 0.5 to 20 Hz depending
on the amplitude of the vibration. It is the customers responsibility to contract a vibration consultant
or qualified engineer to implement design modifications to meet the specific limits, However, it is
ultimately the customer/architect/engineer responsibility to design the site solution.
8.5.1Steady State Vibration
The maximum steady state vibration transmitted through the floor should not exceed 10-3 m/s2 rms
maximum single frequency above ambient baseline from 0.5 to 80 Hz (measured in any 1 hour
during a normal operating period).
8.5.2Transient Vibration
The behavioral characteristics must be such that any measurable transient disturbance must also
be minimized to less than 0.01 m/s
To minimize the interference, the CT equipment should be placed on a solid floor, located as far as
possible from the following vibration sources:
•Parking lots•Roadways•Subways
•Trains•Hallways•Elevators
•Heliports•Hospital power plants containing pumps, motors, air handling
equipment and air conditioning units
8.6Walls: Scan Window
The recommended patient viewing window dimensions are 1219 mm wide by 1067 mm high (48 in.
x 42 in. ). The location of the window is dependent on the position of Operator Workspace position.
Consult Section 10.0 of this chapter and a qualified radiological health physicist for radiation
protection requirements of glass (lead content and thickness).
Note: The operator at the Operator Workspace must be able to view the patient during a scan.
8.7Ceiling Requirement
The weight of "Boom in a room LCD monitor" assy is 50 kg., and ceiling shall have enough strength
against the specification.
Broad-band is the standard network connection and is required for BrightSpeed Series systems. (A
dial-up modem is optional.) A 1000 baseT high-speed network is desired, with 100 baseT network
service acceptable. Broad-band connections should use one of the following Category 5 patch
cables:
CAT NumGE Part NumLength
K9000WB2215028-1020 m
K9000KP2215028-510 m
K9000JR2215028-45 m
K9000WA2215028-93 m
The CT system is connected to the network through the Console.
•A patch cable (not to exceed 3.05 m (10 ft. ) should be provided by the customer, and it is used
to connect the console to a wall box. (See Notes on
•Some customer-site units may require cable duct-work or conduit to route connecting network
cables to the workstation, camera and console.
•The run from the hospital switch to the CT wall outlet must not exceed 88m (290 ft. ). Bandwidth
performance is degraded when the length reaches 91m (300 ft. ) or greater.
•For the optional modem: Two phone lines should be provided by the facility. One line is for
use with a modem and must be an analog line. The second line is a voice only line.
The United States network connectivity requirement for this product is broad-band. The US process
relies on the Project Manager Installation to select a Customer Champion and identify an IT contact
for the site. Together, those individuals then complete a site assessment to gauge what tasks are
needed to fulfill the connection.
Anyone can contact the GE Connectivity team at 800.321.7937, Option #3, with questions.
Provide GE Healthcare Installation Project Manager with an accurate site address, telephone
number, contact name, and e-mail address for the:
•Customer Champion
-Coordinate VPN activities between Radiology/Cardiology and the Information Technology
(IT) departments
-Act as a focal point in assuring site broad-band infrastructure meets GE Healthcare
requirements for connection as determined by a mutual assessment with the GE
Healthcare Connectivity team.
•Materials used for construction of walls, floors, ceiling, doors, and windows
•Access to surrounding scan room areas
•Equipment in surrounding scan room areas (e.g., film developer, film storage)
Figure 4-22 depicts measurable radiation levels within the scanning room while scanning a 32 cm
CTDI phantom (body) and a 20 cm water phantom (head) with the technique shown. The mAs, kV
and aperture scaling factors shown in Table 4-11 can be used to adjust exposure levels to the scan
technique used at the site.
Note: Actual measurements can vary. All measurements have an accuracy of ± 20% because of
measurement equipment, technique, and system-to-system variation.
Use the correction factors shown in Table 4-11 to adjust exposure levels to the usual scan
technique at your site.
CHANGED PARAMETERMULTIPLICATION FACTOR
mAsnew mAs/100
80 kV0.21
120 kV0.71
140 kV1.0
4 x 3.75mm images0.82
16 x 0.625 LD
8 x 1.25 LD
4 X 2.5 LD
Fluro 5mm
4 x 1.25 LD
5mm (1i)
Fluro 2.5 mm
1 x 1.25mm images0.20
2 x 0.625 LD
1 x 1.25
Table 4-11 Shielding Requirements Scaling
NOTICE The units of measure used for radiation levels have been changed in this publication, from
mR (millirads) to Gy (micrograys). The conversion factor is:
1 mR = 8.69 Gy
0.59
0.40
0.10
4 – Room Planning
Chapter 4 - Room PlanningPage 91
Page 92
GE HEALTHCARE
0.33
0.33
0.65
0.65
1.3
1.3
2.6
2.6
0.330.330.650.651.31.32.62.6
HEAD PHANTOM
Technique:
140 kV
100mA
1 Sec
4 x 5.00mm
Technique:
140 kV
100mA
1 Sec
4 x 5.00mm
50cm
50cm
50cm
50cm
HEAD PHANTOM
ISO–Contour Levels: 0.33, 0.65, 1.3 and 2.6 µGy/Scan
ISO–Contour Levels: 0.33, 0.65, 1.3 and 2.6 µGy/Scan
Ratings and duty cycles of CT subsystems apply if site environment meets the standards of this
section. Maintain environmental conditions listed below at all times – including, for example,
overnight, weekends and holidays. Shut down the CT system if air conditioning is not working.
When system is shut down for major repair, air conditioning may be shut down also.
NOTICE Silver, copper, gold films used in the CT system are especially sensitive to the presence of
sulfide, chloride and nitrate contaminates. Sulfur is the most damaging. If high levels of
contaminates exist site may want to consider appropriate air filtration systems.
Section 1.0
Temperature and Humidity Specifications
Environmental specifications apply to the table, gantry, power distribution unit, and operating
console.
NOTICE System Operation and Image Quality may be affected, if environmental specifications are
exceeded.
1.1Temperature (Scan Room & Control Room)
Maximum allowable ambient room temperature:26º C (79º F)
Recommended ambient room temperature:22º C (72º F)
Minimum allowable ambient room temperature:18º C (64º F)
Maximum allowable ambient room temperature rate of change:3º C/hr. (5º F/hr. )
Equipment Room: If a separate equipment room is used to house the PDU, the allowable
temperature range is 64º - 79º F (18º - 26º C).
Maximum allowable relative humidity rate change:5% per hour
1.3Other Guidelines
•To help determine the hospital room environmental conditions, a temperature and humidity
recorder may be temporarily installed close to where the system will be installed. Note
readings before and after installation, to verify the true temperature and humidity in your
environment.
•Consider heating, ventilating, air conditioning (HVAC) needs and redundancy. An air
conditioner with two compressor units, rather than one, may prevent system downtime. A
back-up (redundant) air conditioner permits CT system operation during an extended repair of
the primary air conditioner.
Page 98 Section 1.0 - Temperature and Humidity Specifications
Use Table 5-1 to assist in cooling requirements planning. Over half the cooling used by your
scanner is required for gantry operation. Locate a wall air-conditioning vent at floor level beside and
behind gantry to meet both gantry cooling needs and provide patient comfort. Do not locate any
cooling vents directly above the gantry. Air returns above the gantry are recommended.
SYSTEM COMPONENTBTU/HRWATT
1. Gantry recommended (See NOTE 1)18,7665,500
2. HPower Table / GT1700 Table682/1023200/300
3. Power distribution unit5,1181,500
Recommended Scan Room Subtotal (see notes):24,566/24,9077,200/7,300
Note: If power sub-stations exist under or above the scan room, or near the control room, consider EMI
testing to determine if your proposed room meets the published acceptable EMI room limits. This
also includes high voltage lines under the scan or control room floor.
4.1Gantry and Table
Locate gantry in ambient static magnetic fields of less than 10-4 tesla (1,000 milligauss) to
guarantee specified imaging performance. Ambient AC magnetic fields must be below 10
(10 milligauss) peak.
-6
tesla
WARNING
REQUISITES
FOR ROOM
GANTRY & TABLE ARE ALLOWED TO BE INSTALLED ONLY IN X-RAY PROTECTED
ROOMS, WHICH PROVIDE AN ATTENUATION OF AT LEAST 12dB FOR RADIO
DISTURBANCES FROM 30 MHz TO 1 GHz.
(The Warning statement above is specified by IEC 60601-1-2, First Edition, 1993)
4.2Color Monitor
Locate color monitors in ambient static magnetic fields of less than 5 x 10-5 tesla (100 milligauss)
to guarantee color purity and display geometry. See Figure 5-1.
4.3Console / Computer Equipment
Locate computer equipment in ambient static magnetic fields of less than 10-3 tesla (10,000
milligauss) to guarantee data integrity. See Figure 5-1.
4.4Magnetic Media
Locate magnetic media in ambient static magnetic fields of less than 10-3 tesla (10,000 milligauss).
4.5PDU
The PDU produces an electromagnetic field that radiates outward from its cabinet in all directions.
Do not place the gantry or patient table within 0.3 meters (12 in.) of the edge of the Power
Distribution Unit. Do NOT place other sensitive electronics (e.g. the computer equipment) within 1.0
meters (39 in.) of the edge of the Power Distribution Unit in any direction, including above or below
it. See Figure 5-1.
Note: The UPS is not classified as sensitive electronics.