Fluke Biomedical warrants this instrument against defects in materials and workmanship for one full year from the date of original purchase. During the warranty
period, we will repair or, at our option, replace at no charge a product that proves
to be defective, provided you return the product, shipping prepaid, to Fluke Biomedical. This warranty does not apply if the product has been damaged by accident or misuse or as the result of service or modification by other than Fluke Biomedical. IN NO EVENT SHALL FLUKE BIOMEDICAL BE LIABLE FOR
CONSEQUENTIAL DAMAGES.
Only serialized products and their accessory items (those products and items bearing a distinct serial number tag) are covered under this one-year warranty.
PHYSICAL DAMAGE CAUSED BY MISUSE OR PHYSICAL ABUSE IS NOT
COVERED UNDER THE WARRANTY. Items such as cables and nonserialized
modules are not covered under this warranty.
Recalibration of instruments is not covered under the warranty.
This warranty gives you specific legal rights, and you may also have other rights
which vary from state to state, province to province, or country to country. This
warranty is limited to repairing the instrument to Fluke Biomedical’s specifications.
Warranty Disclaimer
Should you elect to have your instrument serviced and/or calibrated by someone
other than Fluke Biomedical, please be advised that the original warranty covering
your product becomes void when the tamper-resistant Quality Seal is removed or
broken without proper factory authorization. We strongly recommend, therefore,
that you send your instrument to Fluke Biomedical for factory service and calibration, especially during the original warranty period.
Fluke Biomedical agrees to a limited copyright release that allows you to reproduce manuals and
other printed materials for use in service training programs and other technical publications. If you
would like other reproductions or distributions, submit a written request to Fluke Biomedical.
Unpacking and Inspection
Follow standard receiving practices upon receipt of the instrument. Check the shipping carton for
damage. If damage is found, stop unpacking the instrument. Notify the carrier and ask for an agent to
be present while the instrument is unpacked. There are no special unpacking instructions, but be careful not to damage the instrument when unpacking it. Inspect the instrument for physical damage such
as bent or broken parts, dents, or scratches.
Technical Support
For application support or answers to technical questions, either email techser-
vices@flukebiomedical.com or call 1-800- 648-7952 or 1-425-446-6945.
Claims
Our routine method of shipment is via common carrier, FOB origin. Upon delivery, if physical damage is found, retain all packing materials in their original condition and contact the carrier immediately to file a claim. If the instrument is delivered in good physical condition but does not operate
within specifications, or if there are any other problems not caused by shipping damage, please contact Fluke Biomedical or your local sales representative.
Standard Terms and Conditions
Refunds and Credits
Please note that only serialized products and their accessory items (i.e., products and items
bearing a distinct serial number tag) are eligible for partial refund and/or credit. Nonserialized
parts and accessory items (e.g., cables, carrying cases, auxiliary modules, etc.) are not eligible
for return or refund. Only products returned within 90 days from the date of original purchase are
eligible for refund/credit. In order to receive a partial refund/credit of a product purchase price on a serialized product, the product must not have been damaged by the customer or by the carrier chosen by
the customer to return the goods, and the product must be returned complete (meaning with all manuals, cables, accessories, etc.) and in “as new” and resalable condition. Products not returned within 90
days of purchase, or products which are not in “as new” and resalable condition, are not eligible for
credit return and will be returned to the customer. The Return Procedure (see below) must be followed to assure prompt refund/credit.
Restocking Charges
Products returned within 30 days of original purchase are subject to a minimum restocking fee of 15
%. Products returned in excess of 30 days after purchase, but prior to 90 days, are subject to a minimum restocking fee of 20 %. Additional charges for damage and/or missing parts and accessories will
be applied to all returns.
Return Procedure
All items being returned (including all warranty-claim shipments) must be sent freight-prepaid to our
factory location. When you return an instrument to Fluke Biomedical, we recommend using United
Parcel Service, Federal Express, or Air Parcel Post. We also recommend that you insure your shipment for its actual replacement cost. Fluke Biomedical will not be responsible for lost shipments or
instruments that are received in damaged condition due to improper packaging or handling.
Use the original carton and packaging material for shipment. If they are not available, we recommend
the following guide for repackaging:
Use a double-walled carton of sufficient strength for the weight being shipped.
Use heavy paper or cardboard to protect all instrument surfaces. Use nonabrasive material
around all projecting parts.
Use at least four inches of tightly packed, industry-approved, shock-absorbent ma-
terial around the instrument.
Returns for partial refund/credit:
Every product returned for refund/credit must be accompanied by a Return Material Authorization
(RMA) number, obtained from our Order Entry Group at 1-800-648-7952 or 1-425-446-6945.
Repair and calibration:
To find the nearest service center, go to www.flukebiomedical.com/service
In the U.S.A.:
Cleveland Calibration Lab
Tel: 1-800-850-4606
Email: globalcal@flukebiomedical.com
In Europe, Middle East, and Africa:
Eindhoven Calibration Lab
Tel: +31-402-675300
Email: ServiceDesk@fluke.com
In Asia:
Everett Calibration Lab
Tel: +425-446-6945
Email: service.international@fluke.com
, or
Certification
This instrument was thoroughly tested and inspected. It was found to meet Fluke Biomedical’s manufacturing specifications when it was shipped from the factory. Calibration measurements are traceable
to the National Institute of Standards and Technology (NIST). Devices for which there are no NIST
calibration standards are measured against in-house performance standards using accepted test procedures.
WARNING
Unauthorized user modifications or application beyond the published specifications may result in electrical shock hazards or improper operation. Fluke Biomedical will not be responsible for any injuries sustained due to unauthorized equipment modifications.
Restrictions and Liabilities
Information in this document is subject to change and does not represent a commitment by
Fluke Biomedical. Changes made to the information in this document will be incorporated in
new editions of the publication. No responsibility is assumed by Fluke Biomedical for the use
or reliability of software or equipment that is not supplied by Fluke Biomedical, or by its affiliated dealers.
Manufacturing Location
The RF303 Electrosurgical Analyzer is manufactured in Everett, Washington by Fluke Biomedical, 6920 Seaway Blvd., Everett, WA, U.S.A.
Table of Contents
1 Introduction and Specifications.............................................. 1-1
The RF303 Electrosurgical Analyzer, hereafter referred to as the “Analyzer”,
tests electrosurgical units (ESU) for generator output and high frequency (HF)
leakage. It is compatible with both isolated and earth/ground-referenced types
of electrosurgical units. You can test both the high-level monopolar and the
low-level bipolar ESU outputs using this versatile Analyzer.
The Analyzer uses a precision high-voltage capacitive attenuator to sample the
applied ESU signal. You can use this attenuated HF voltage and the selected
test load resistance value to derive the true-rms values of both current and
wattage.
The Analyzer internal test load simulates the range of resistance encountered
during surgical procedures. Additionally, a second, 200 ohm (e) auxiliary test
load resistance is built-in to analyze earth/ground-referenced ESUs as specified
in the International Standard IEC 601-2-2.
The exclusive use of non-conductive, high-impact plastic case material
minimizes extraneous high frequency leakages within the Analyzer.
General Safety Information
This Analyzer complies with safety and technical requirements described in
the following directives:
• UL 3101-1
• CAN/CSA C22.2 No. 1010.1 (1992)
• EC 73/23/EEC EN 61010–1
• ANSI / AAMI HF–18-1986
• IEC 601-2–2
• IEC 1289-1
• IEC 1289-2
A Warning identifies hazardous conditions and actions that could cause
bodily harm or death.
A Caution identifies conditions and actions that could damage the Analyzer,
the equipment under test, or cause permanent loss of data.
1-3
RF303
Operators Manual
Symbols
Table 1-1 describes the symbols used in this document.
Table 1-1. Symbols
Symbol Description Symbol Description
W
$
t
Risk of danger. Important
information. See manual.
Conforms to relevant
Canadian and U.S.
standards
Underwriters Laboratories
listed product
Indicates that a terminal is
connected to the chassis
when such a connection is
not apparent.
J Earth ground
X
P
B AC (Alternating Current)
F DC (Direct Current)
~
Hazardous voltage. Risk
of electrical shock.
Conforms to European
Union directives
Do not dispose of this
product as unsorted
municipal waste. Contact
Fluke or a qualified
recycler for disposal.
Warnings and Cautions
When testing electrosurgical units, observe the following to ensure operator
safety and maintain integrity of the high frequency (HF) measurement.
WX Warning
To avoid possible electric shock, burning of the skin, or personal injury, follow these guidelines:
• Use only test leads supplied with the Analyzer to test the
ESU. These test leads utilize a shrouded 4mm plug to
limit exposure to the high-voltage and high frequency
ESU signal. The retractable ends of these leads are for
use on ESU only.
1-4
Introduction and SpecificationsGeneral Safety Information
• Do not plug in or remove a test lead from either the ESU
or the Analyzer while the ESU generator is activated (or
keyed). This high frequency ESU signal can be several
thousand volts in amplitude when the output is opencircuited.
• Whenever practical during testing, activate the ESU
generator output using the foot switch supplied with the
ESU.
• No probes or accessories supplied with the analyzer are
intended for handheld use. Set up using the safety test
leads and stand clear when activating the ESU with the
footswitch.
• Place the Analyzer on an insulated, non-conductive work
surface to limit possible HF current paths to earth
ground.
• Routinely inspect test leads for wear and tear. Repair or
replace the test leads to maintain operator safety and
Analyzer performance.
1
Note
To ensure accuracy of measurement, follow these guidelines:
• Whenever practical during testing, place test leads carrying the
ESU signals in parallel, approximately 0.5 meters apart, to limit
capacitive coupling.
• Avoid crossing or tangling test lead cables during use and do not
drape them across conductive, grounded surfaces. Due to their
length, erroneously high HF readings may result.
Electromagnetic Interference and Susceptibility
Like all similar equipment, this equipment generates, uses, and can radiate
radio frequency energy and, if not installed and used in accordance with the
instruction manual, may cause harmful interference to radio communications.
Operation of this equipment in a residential area could cause interference, in
which case the user will be required to correct the interference and bear any
1-5
RF303
Operators Manual
costs. The limits established by the following organizations are designed to
provide reasonable protection against harmful interference when the
equipment is operated in a commercial environment.
The Analyzer has been tested by independent testing laboratories and found to
meet the following requirements:
EC Directive 89/336/EEC EN 50081-1 Emissions
Radiated Emissions and Line Conducted Emissions. Verification was to the
limits and methods of EN 55011. The device is classified as EN 55011, Group
A.
EC Directive 89/336/EEC EN 50082-1 Immunity
Electrostatic Discharge Susceptibility, Radiated Susceptibility, and Electrical
Fast Transient/Burst Susceptibility. Verification of compliance was conducted
to the limits and methods of EN 50082-1:1992, IEC 1000-4-2; EN 61000-4-3;
IEC 1000-4-4; EN 61000-4-5; EN 61000-4-6; EN 61000-4-11.
USA Federal Communications Commission
This equipment has been found to comply with the limits for a Class A digital
device, pursuant to Part 15 of the FCC Rules.
Canadian Department of Communications
This digital apparatus does not exceed Class A limits for radio emissions from
digital apparatus set out in the Radio Interference Regulations of the Canadian
Department of Communications.
Le present appareil numerique n'met pas du bruits radioelectriques depassant
les limites applicables aux appareils numerique de la Class A prescrites dans le
Reglement sur le brouillage radioelectrique edicte par le ministere des
Communications du Canada.
1-6
Introduction and SpecificationsControl and Interface Panels
1
Control and Interface Panels
Figure 1-1 and Table 1-2 describe the controls and interfaces of the Analyzer.
19
9
20
1
2
3
5
4
6
7
8
10
RF-303
ELECTROSURGICAL ANALYZER
11
12
Figure 1-1. Analyzer Control and Interface Panels
Table 1-2. Controls and Connections
13
18
17
16
1514
exz14.eps
Item Name / Description
1 Display
Backlit, numeric, 4-digit LCD
2 Power Indicator (WATTS) Lamp
Displays reading in watts.
3 Current Indicator (mA) Lamp
Displays readings in milliamperes (mA).
1-7
RF303
Operators Manual
Table 1-2 Controls and Connections (cont.)
Item Name / Description
4 Test Load (OHMS) Lamp
Displays resistance in ohms.
5 Mode Selection (MODE SELECT ENT) Pushbutton
Toggles the display between Power (in watts) and Current (in mA).
6 Increase Test Load (OHMS SELECT +) Pushbutton
7 Decrease Test Load (OHMS SELECT -) Pushbutton
8 Carrying Handle
9 Battery Status Lamp
10 Scope Output
BNC connector
11 Measuring Resistance/HF Meter
All measurements made through these inputs.
12 Earth Connections
Provides earth reference for HF Leakage tests.
13 HF Load Resistance
Auxiliary test load for earth/ground-referenced Type BF Tests 2 and 3.
14 Battery Ground / Signal Earth Ground
15 Power Cord Inlet
16 Fuse Cover
Both power mains fuses are located behind this panel.
17 Power On/Off Switch
18 Ventilation Air Outlet
19 Ventilation Air Inlet
20 RS232 Port
1-8
Introduction and Specifications
Instrument Specifications
1
Instrument Specifications
Modes of Operation
Line Powered (Battery Charge and Maintenance Charge)
Battery Operation
Offline (Battery Charge and Maintenance Charge)
Displayed Parameters
Power (Watts)
HF Current (milliamperes)
Test Load (ohms)
Test Performed
Generator Output
HF Leakage ........................................................ Performs HF leakage tests to IEC 601
Resolution....................................................... 1 to 400 W / Resolution: 0.1 W
Maximum power input .................................... 400 W rms
Accuracy..................................................... ± 5 % of reading or ± 3 watts,
HF Current
Range ......................................................... 30 to 2500 mA rms, Resolution: 1 mA
Accuracy..................................................... ± 2.5 % of reading or ± 15 mA,
Bandwidth/System Response
Bandwidth of rms converter circuit (1 % accuracy)
Flat response.................................................. 10 kHz to 10 MHz
-3 dB points..................................................... 1 kHz to 20 MHz
System Response (measurement circuitry and selected test load):
-3 dB points..................................................... 1 kHz to 10 MHz @ 300 e
2-2, 1289-2, ANSI/AAMI standards:
Type BF Test 1 – Earth referenced
monopolar output Type CF/Bipolar –
Isolated monopolar or bipolar output
attenuator samples applied ESU
signal. This directly measured HF
voltage and the selected test load
resistance value utilized to derive the
true-rms values of both current and
wattage readings.