Midmark Barrier-Free 626, Barrier-Free 626-001, Barrier-Free 626-002 User Manual
Style P
Barrier-Free® Exam Chair
For Models:
626 (-001, -002)
User Guide
TP202 20-42-FO-00014 Rev A2 C2169
003-10026-99 Rev. AA3 (03/03/18)
English
Español
Français
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003-10026-99 © Midmark Corporation 2017
TP202 20-42-FO-00014 Rev A1 C2169
Model / Serial Number:
Date of Purchase:
Midmark Authorized Service
Company:
Dealer:
Product Information
Model / Serial Number Label Located
on the Back Mounting Frame
(exact location may vary)
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Table of Contents
Safety Symbols ......................................................................................................................4
Product Registration .............................................................................................................5
Transportation / Storage Conditions ...................................................................................5
Operating Conditions ............................................................................................................5
Disposal of Equipment ..........................................................................................................5
Compliance Information .......................................................................................................6
Intended Use ..........................................................................................................................7
Electrical Requirements .......................................................................................................7
Electromagnetic Interference ...............................................................................................7
Safety Instructions .................................................................................................................9
Operation
Active Sensing Technology
TM
.............................................................................................11
Base / Back Functions ........................................................................................................12
Programmable ’Home’ Function ........................................................................................13
Quick Exam® Function ........................................................................................................14
Paper Roll & Tear Strap ......................................................................................................15
Stirrups ..................................................................................................................................16
Footrest & Treatment Pan ..................................................................................................17
Drawer Heater ......................................................................................................................18
Upholstery Heater (626-002) .............................................................................................19
Pelvic Tilt ..............................................................................................................................20
Duplex Receptacles ............................................................................................................21
Clean Assist™ Roller System ...........................................................................................22
Maintenance
Calling for Service ...............................................................................................................23
Cleaning ................................................................................................................................23
Troubleshooting ...................................................................................................................24
Specications
Specications Chart ............................................................................................................25
Model Identication / Compliance Chart ..........................................................................26
Range of Motion ..................................................................................................................27
Dimensions: .......................................................................................................................28
Warranty Information
Limited Warranty .................................................................................................................29
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Catalogue Number
Manufacturer
Serial Number
Stop
WARNING
Indicates a potentially hazardous situation which could result in serious injury.
Important Information - Safety Symbols
Caution
Indicates a potentially hazardous situation which may result in minor or moderate injury.
It may also be used to alert against unsafe practices
Equipment Alert
Indicates a situation which could result in equipment damage.
Protective earth ground
Proper shipping orientation
Fragile
Type B, Applied Part
(Standard Upholstery)
Patient Weight Limit
xxx kg
xxx lbs
Fuse rating specication
Dangerous voltage / shock hazard
Maximum stacking height
(palletted units)
Keep dry
Duty Cycle (motor run time)
30 seconds ON, 5 minutes OFF
Note
Amplifies a procedure, practice, or condition.
Refer to manual
Symbol Glossary
The heated upholstery is a
Type BF, Applied Part.
Do not penetrate upholstery
with sharp objects, such as
needles, knives, etc.
Operating Instructions
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Transportation / Storage Conditions
Ambient Temperature Range: .....................................-30°C to +60°C (-22°F to +140°F)
Relative Humidity........................................................10% to 90% (non-condensing)
Operating Conditions
Ambient Temperature Range: .....................................+10°C to +40°C (+50°F to +104°F)
Relative Humidity........................................................30% to 75% (non-condensing)
Altitude........................................................................3000m or less
Disposal of Equipment
At the end of product life, the chair, accessories, and other consumable goods may have become
contaminated due to normal medical use. Consult local codes and ordinances for proper disposal of
equipment, accessories and other consumable goods.
Product Registration
To register your product, go to www.midmark.com
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Compliance Information
FCC Compliance Statement
This equipment has been tested and found to comply with the limits for a class A digital device, pursuant
to part 15 of the FCC rules. These limits are designed to provide reasonable protection against harmful
interference when the equipment is operated in a commercial environment. 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 is likely to cause harmful interference in which case the user will be required to correct
the interference at their own expense.
Any modications to this product may violate the rules of the Federal Communications Commission and
make operation of the product unlawful.
IC Compliance Statement
Interference
“This device complies with Industry Canada license-exempt RSS standard(s). Operation is subject to the
following two conditions: (1) this device may not cause interference, and (2) this device must accept any
interference, including interference that may cause undesired operation of the device.”
“Le présent appareil est conforme aux CNR ďIndustrie Canada applicables aux appareils radio exempts
de licence. Ľexploitation est autorisée aux deux conditions suivantes: (1) ľappareil ne doit pas produire
de brouillage, et (2) ľutilisateur de ľappareil doit accepter tout brouillage radioélectrique subi, même si le
brouillage est susceptible ďen compromettre le fonctionnement.”
Antennas
“Under Industry Canada regulations, this radio transmitter may only operate using an antenna of a type
and maximum (or lesser) gain approved for the transmitter by Industry Canada. To reduce potential
radio interference to other users, the antenna type and its gain should be so chosen that the equivalent
isotropically radiated power (e.i.r.p.) is not more than that necessary for successful communication.”
“Conformément à la réglementation ďIndustrie Canada, le présent émetteur radio peut fonctionner avec une
antenne ďun type et ďun gain maximal (ou inférieur) approuvé pour ľémetteur par Industrie Canada. Dans
le but de réduire les risques de brouillage radioélectrique à ľintention des autres utilisateurs, il faut choisir le
type ďantenne et son gain de sorte que la puissance isotrope rayonnée équivalente (p.i.r.e.) ne dépasse pas
ľintensité nécessaire à ľétablissement ďune communication satisfaisante.”
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Electromagnetic Interference
This product is designed and built to minimize electromagnetic interference with other devices. However, if
interference is noticed between another device and this product:
• Remove interfering device from room
• Plug chair into isolated circuit
• Increase separation between chair and interfering device
• Contact Midmark if interference persists
Electrical Requirements
Before connecting the Midmark device power cord into an electrical power source outlet, it is recommended
to contact a local licensed electrician or a local Authority Having Jurisdiction over the internal building power
distribution to verify that the device when powered up will comply with all local electrical codes. Use the
electrical power rating marked on the device when determining the appropriate electrical branch circuit and
outlet requirements. For 115V rated device models with a current rating at or above 12 Amps, a dedicated
branch circuit may be required if the branch circuit protection is provided by a 15 Amp breaker.
Intended Use
The examination chair is intended to be used as a chair / table to provide positioning and support of patients
during general examination procedures conducted by medical professionals.
Equipement Alart
Portable RF communications equipment (including peripherals such as antenna cables
and external antennas) should be used no closer than 30 cm (12 inches) to any part of the
Exam Chair including cables specified by the manufacturer. Otherwise, degradation of the
performance of this equipment could result.
Caution
To completely isolate the chair from electrical mains supply, power cord must be unplugged.
Caution
Prior to use of high frequency surgical devices or endocardial catheters, consult the operating
instructions for those devices. Failure to comply may result in electric shock or burns to the
patient.
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Immunity Test Immunity Test Level
Electrostatic Discharge ± 8 kV Contact, ±15 kV Air
Radiated RF EM Fields 3V/m
80MHz-2.7 GHz 80% AM at 1kHz
Rated Power Frequency Magnetic Fields 30 A/m
Electrical Fast Transients ±2 kV at 100kHz repetition frequency
Surges Line to Line: ±1 kV
Line to Ground: ±2 kV
Conducted RF 3V: 0.15MHz -80MHz
6V in ISM Bands between 0.15MHz - 80MHz
80% AM at 1kHz
Voltage Dips 0 % UT; 0,5 cycle
At 0°, 45°, 90°, 135°, 180°, 225°, 270° and 315°
0 % UT; 1 cycle
and
70 % UT; 25/30 cycles
Single phase: at 0°
Voltage Interruptions 0 % UT; 250/300 cycle
Note
The emissions characteristics of this equipment make it suitable for use in industrial areas and
hospitals. The exam chair is not intended to be used in a residential environment.
EMC - Manufacturer’s Declaration and Guidance
Radiated Test Radiated Test Level
Conducted and Radiated RF Emissions CISPR 11 Group 1 Class A
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Safety Instructions
Warning
No modification of this equipment is allowed.
Warning
Connecting equipment to the multiple socket outlet effectively leads to creating a Medical
Electrical System and the result can be a reduced level of safety.
Warning
To avoid a fire hazard or risk of electric shock, this equipment must only be connected to a
supply mains with protective earth ground.
Warning
Ensure that the surrounding area is clear of obstructions prior to each use. Otherwise improper
operation and serious injury could occur.
Warning
Use of accessories, transducers and cables other than those specified or provided by the
manufacturer of this equipment could result in increased electromagnetic emissions or
decreased electromagnetic immunity of this equipment and result in improper operation.
WARNING
Equipment is not suitable for use in the presence of a flammable anesthetic mixture.
Clarification: Equipment is suitable for use in the presence of oxygen, air, or nitrous oxide.
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Safety Instructions - continued
At the chair’s lowest height [14.6 in. (37 cm)] w/ compressed foam, the clearance between
the bottom of the drawer and the oor is approximately 0.37 in. (0.94 cm). Make sure
patient (esp. feet) and all objects are clear of this area before lowering chair.
If the chair malfunctions, immediately release controller, unplug the chair power cord, and
assist the patient from the chair. If chair continues to malfunction, call for service.
Failure to comply with these instructions may result in injury to patient and/or damage to
equipment.
Clearance
Approx. 0,94 cm (0,37 in.)
Warning
Be sure that all personnel and equipment are clear of the chair before
activating any function. Failure to do so could result in personal injury.
Equipment Alert
Chair must be positioned in normal use such that the power
cords can be easily accessed to unplug.
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Operation
Active Sensing Technology
TM
The Active Sensing TechnologyTM prevents the chair from moving Down if the bottom of the drawer contacts
another object. If the Active Sensing TechnologyTM is activated, it will sound a series of “Beeps,” disable the
Base Down function and move chair in the Base Up direction. To resume Base Down operation, remove
object from under the bottom of the drawer and press the Base Up / Down buttons on controller.
Warning
Be sure that all personnel and equipment are clear of the chair before
activating any function. Failure to do so could result in personal injury.
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Back
Function
Stop
Operation - continued
Base / Back Functions
To operate the Base / Back functions...
Press & hold the Up or Down arrow button for the
desired function.
Note: The chair automatically stops at its maximum and
minimum height. At anytime, the Stop button can be
pressed to terminate movement.
Back Function
Base Function
Stop
Base
Function
Attention!
The Active Sensing Technology
TM
will stop the Base Down function and retract Up if the bottom of
the drawer contacts another object.
(You will hear a series of “Beeps” if the Active Sensing TechnologyTM is activated.)
To resume Base Down operation:
Remove object from under the bottom of the drawer.
Press Base Down button.
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Programmable ’Home’ Function
The Home function automatically commands the chair to a programmed position.
The Home function is factory preset to automatically lower the chair height to 17 inches (43 cm)
and raise the Back angle to 80 degrees.
To activate the Home function...
Press & release the Home button.
Note: At any time, ANY button can be pressed
to terminate movement.
Home
Stop
Home
Stop
To program the Home function...
a) Press the Base Up / Down button to move the Base to the desired height.
b) Press the Back Up / Down button to move the Back to the desired angle.
c) Press the Stop button, then the Home button and hold simultaneously for
three to four seconds.
Note: You will hear an audible tone when the new ’Home’ position is saved.
Note
An audible tone will sound when the Home button is pressed to indicate auto-movement.
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Quick Exam
®
Stop
To program the Quick Exam® function...
a) Press the Base Up / Down button to move the Base to the desired height.
b) Press the Back Up / Down button to move the Back to the desired angle.
c) Press the Stop button, then the Quick Exam® button and hold simultaneously
for three to four seconds.
Note: You will hear an audible tone when the new Quick Exam® position is saved.
Quick Exam® Function
The Quick Exam® function automatically commands the chair to a programmed position.
The Quick Exam® function is factory preset to automatically raise the chair height to 34 inches (86 cm) and
raise the Back angle to 80 degrees.
To activate the Quick Exam® function...
Press & release the Quick Exam® button.
Note: At any time, ANY button can be pressed to
terminate movement.
Stop
Quick Exam
®
Note
An audible tone will sound when the Quick Exam® button is pressed to indicate auto-movement.
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To install paper roll...
Insert rod ends into sockets
under head end of upholstery.
To install paper tear strap...
Attach strap to snaps on each side of chair.
Warning
To avoid injury, do not put head or extremities under the paper tear strap.
Note
One additional paper roll may be stored under the back section.
Paper Roll & Tear Strap
Paper Roll Size (maximum): ....................................................... 24 in. wide x 3.5/8 in. diameter
(61 cm x 9.2 cm)
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To position the stirrups...
A) Pull the stirrup out, then unfold.
B) Lift the stirrup slightly, then move it left or right as desired.
C) Release stirrup to lock in position.
Stirrups
Caution
Be sure the stirrups are locked in place before using.
The stirrups will not support the patient’s entire weight.
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To extend footrest...
Pull footrest out to desired position.
Footrest & Treatment Pan
To access the treatment pan...
Pull treatment pan out to desired position.
Warning
Do not use footrest to support patient’s entire weight.
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To turn the drawer heater ON / OFF...
Press and release the drawer heater switch.
Note: Switch will illuminate when heater is ON.
Drawer Heater
Switch
Drawer Heater
The drawer heater warms to 92ºF (33ºC) to 112ºF (44ºC) measured at the center of the drawer at room
temperature and nominal input voltage.
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Upholstery Heater (626-002)
Upholstery Heater
Switch
To turn the upholstery heater ON / OFF...
Press and release the upholstery heater switch once
for the LOW setting and twice for the High setting.
Pressing the heater switch a third time will turn
upholstery heater off.
Note: Switch will illuminate “Dim Green” on the LOW setting, and
illuminate “Bright Green” on the HIGH setting.
Caution
Use of the upholstery heater in combination with other
heating devices could cause elevated body temperature.
The nominal surface temperature of the LOW setting is approximately 95° +/- 5° F, and the nominal surface
temperature of the HIGH setting is approximately 102° +/- 5° F at an ambient temperature of 70° +/- 2° F.
There will be approximately a dierence of 7° +/- 2° F between the high and low setting.
The upholstery heater will automatically shut o after ten hours of operation. It takes the upholstery
approximately 20 to 25 minutes to reach 99° F from an ambient temperature of 73° F.
Note
Harnesses protruding out of the table from underneath the
back weldment are to be used for heated upholstery only.
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Pelvic Support
To elevate seat section...
Lift seat until pelvic support drops into place.
To return seat section to flat position...
A) Lift seat section slightly.
B) Pivot pelvic support handle upward.
C) Lower seat section slowly.
Pelvic Tilt
Pelvic Support
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The duplex receptacles on each side of chair provide power for accessories used during medical
procedures. There are two circuit breakers located under the seat section. If the receptacles’ maximum load
is exceeded, the circuit breakers interrupt power to the receptacles.
Maximum Load..........................................................................................115 VAC, 4 amps
Tripped
(no power)
Reset
(power)
Circuit Breakers
To reset the circuit breaker...
Push circuit breaker switch.
Duplex Receptacles
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Equipment Alert
Be sure to activate both control levers.
Note
Control levers will automatically reset to the Clean Assist™
Roller System
disengagement position.
Zero the scale after the chair is moved for cleaning.
Equipment Alert
After Clean Assist™ Roller System has been
activated, disconnect power cord and foot control and
stow away from chair to prevent damage to cords.
Clean Assist™ Roller System
Clean Assist™ Roller
System Engagement
Position
Clean Assist™
Roller System
Equipment Alert
The intended use of the
Clean Assist™ Roller System
is for chair positioning within
the exam room only.
Control levers located under the back section on each side, activate and deactivate the Clean Assist™
Roller System. The rollers are located on each corner of the chair to allow positioning of chair.
Caution
To prevent injury, never activate /
deactivate Clean Assist™ Roller System
or move chair with patient aboard. Use
caution when moving chair.
To deactivate Clean Assist™ Roller System...
A) Move chair to desired location.
B) Reconnect power cord.
C) Raise chair at least 2” to deactivate Clean
Assist™ Roller System.
Note: An audible click will occur to confirm deactivation.
Clean Assist™ Roller
System Disengagement
Position
To activate Clean Assist™ Roller System...
A) Raise back section 30 to 45 degrees.
B) Ensure chair is at least two inches higher than its
lowest position.
C) Move control levers on each side of chair to the
Clean Assist™ Roller System engagement position.
D) Move chair to the lowest position to activate rollers.
WARNING
To avoid risk of fall, the Clean Assist™ Roller
System must be disengaged while a patient
ingresses or egresses the chair
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Maintenance
Calling for Service
If service is required, contact your authorized Midmark dealer. To contact Midmark directly:
1-800-MIDMARK (1-800-643-6275)
8:00 am until 5:00 pm Monday - Friday (EST) [excluding standard U.S. holidays]
Cleaning
Upholstery
Wash your upholstery weekly with a mild liquid soap and water mixture, rinse with clear water
and dry completely to remove disinfection cleaner build-up.
Disinfect your upholstery with a solution of standard bleach and water mixed 1 in 10 (10%) or chlorine based
cleaners. Follow this with a clear water rinse and thorough drying of material. See current CDC Guideline for
Disinfection & Sterilization in Healthcare Facilities.
To minimize damage caused by disinfectant cleaner residue build-up, do not allow disinfectants to pool on
the upholstery surface. Once the approved contact time has been obtained, remove and dry excess liquid
remaining on the surface.
Detailed care and maintenance instructions are included with your product. This information is also available
on www.midmark.com in the Technical library under the User Information tab for your product.
Painted Metal / Plastic Surfaces
Clean the painted metal and plastic surfaces weekly using a clean soft cloth, and mild cleaner.
Preventative Maintenance
Periodically inspect the following areas:
• Power cord(s) should be free of cuts or other visible damage.
• All fasteners should be in place and tightened securely.
• All mechanical functions should operate properly.
Periodically lubricate the back hinge to maintain quiet, smooth, operation (use light machine oil).
Have an authorized service technician inspect your equipment every six months.
Note
Model / serial number information is required when calling for service.
Equipment Alert
The upholstery is resistant to most medicinal-type stains, but may be damaged
by solvents and dyes. Immediately remove any fluids spilled on the upholstery.
Warning
Should damage and or loose parts be identified, the examination chair should be removed from
use and serviced. Failure to do so may result in injury.
Warning
The upholstery should be inspected before each use and replaced
if punctured or otherwise damaged.
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Troubleshooting
Symptom Probable Cause Correction
No functions will operate. Facility supply voltage. Secure power cord connections.
Reset facility circuit breaker.
Chair stops and beeps. Patient weight exceeded 650 lbs. Inform sta that the maximum
patient weight limit is 650 lbs.
No power at chair receptacles. All
other functions work.
Chair circuit breaker(s) tripped. Lift seat section to access circuit
breaker(s), press to reset.
Chair does not move when pressing
Quick Exam
®
button, or does not go
to the correct position.
Quick Exam
®
positioning is user
adjustable and may need to be
reprogrammed.
See Quick Exam® instructions in
this manual.
Active Sensing Technology
TM
activated.
Remove object from under the
bottom of the drawer.
Chair does not move when pressing
’Home’
button, or does not go to the
correct position.
’Home’ positioning is user
adjustable and may need to be
reprogrammed.
See ’Home’ instructions in this
manual.
Active Sensing Technology
TM
activated.
Remove object from under the
bottom of the drawer.
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Specications Chart
Patient Weight (maximum) 650 lbs (295 kg)
Paper Roll (maximum size): 24 in. long x 3.5/8 in. diameter
(61 cm x 9.2 cm)
Range of Motion & Dimensions: [See Range of Motion & Dimensions pages]
Weight of Chair:
w/upholstery
w/packaging & skid (no uph.)
Uph. w/packaging (shipped separately)
475 lbs (215.5 kg)
485 lbs (280 kg)
40 lbs (18.1 kg)
Power Cord Length: 8 ft. (244 cm) long
Electrical Requirements: [See Model Identication / Compliance Chart]
Foot / Hand Control Voltage: 3.3 VDC, SELV (Safety Extra Low Voltage)
Duplex Receptacles Maximum Load: 115 VAC, 4A, 50/60 Hz
Fuses:
IEC inlet fuses
F1 (on Main PC board)
F2 (on Main PC board)
Models w/ upholstery heaters
F1 & F2 (on Uph Heater PC board)
T8AH, 250V, 5 x 20 mm
T250mAH, 250V, 5 x 20 mm
T6.3AH, 250V, 5 x 20 mm
T3.15AH, 250V, 5 x 20 mm
Duty Cycle
(Motor Run Time):
Receptacles, Drawer Heater:
Intermittent Operation
[30 seconds ON / 5 minutes OFF]
Continuous Operation
Classications: Class I, Type B Applied Part, except as noted for
optional heated upholstery,
Intermittent Operation
[30 seconds ON / 5 minutes OFF]
Certications: ES 60601-1:2012, CSA C22.2 No. 60601-1:14;
AAMI/ISO 80601-2-35:2009,
CSA C22.2 No. 80601-2-35:12, IEC 60601-1-2:2014
Optional heated upholstery, Type BF Applied Part,
complies with IEC 80601-2-35
IPX0 Chair
IPX1 Foot Control
IPX2 Heated Upholstery
Transmit / Recieve Frequencies 2.402GHz - 2.480GHz
Specications
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Model Description
Complies To: Electrical Ratings:
ANSI/AAMI
ES60601-1
CAN/CSA-C22.2
No. 60601-1:14
IEC
60601-1-2
NFPA
99
VAC
+/-10%
Amps
Cycles
(Hz)
626-001
Two-function chair (Base / Back)
w/ Duplex Receptacles,
Recessed Rollers,
Pelvic Tilt, & Drawer Heater
• • • •
115 12 50 / 60
626-002
Two-function chair (Base / Back)
w/ Duplex Receptacles,
Recessed Rollers,
Pelvic Tilt, Drawer Heater, &
Heated Upholstery
• • • •
115 12 50 / 60
Fire Code Ratings: All upholstery complies with California Bureau of Home Furnishing Technical Bulletin 117 and California
Code of Regulations, Sect. 93120-93120.12, Title 17. Optional upholstery is available that complies with
California Bureau of Home Furnishing Technical Bulletin 133.
Model Identication / Compliance Chart
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Max.
37 ± 0.5 in.
(94 ± 1.3 cm)
Pelvic Tilt
Max. 7° ± 2°
Min. 1.5°
0° (horizontal) to
+80° ± 5°
Min.
14.6 ± 0.5 in.
(37 ± 1.3 cm)
Range of Motion
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48 in.
(122 cm)
Standard: 8 ft. (2.4 m)
Optional: 3 ft. (91 cm)
10 in.
(25 cm)
Up to:
16 in.
(41 cm)
60 in.
(152 cm)
25 in.
(63.5 cm)
28 in.
(71 cm)
OR
32 in.
(81 cm)
76 in.
(193 cm)
23.5 in.
(60 cm)
Dimensions:
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SCOPE OF WARRANTY Midmark Corporation (“Midmark”) warrants to the original retail purchaser that it will, at Midmark’s option, repair or
replace components of the domestic and international medical products manufactured by Midmark (except for components not warranted
under “Exclusions”) that are defective in material or workmanship under normal use and service. The sole remedy under this limited warranty is the repair or replacement, at Midmark’s option, of the applicable components. This limited warranty shall only apply to defects that are
reported to Midmark within the applicable warranty period and which are determined to exist upon examination by Midmark,. This warranty
extends only to the original retail purchaser of a product and is not transferable or assignable. Replacement components or products may
be used and/or refurbished components or products, provided they are of like quality and speci cations as new components or products.
Midmark warrants to the original retail purchaser that during the applicable warranty period it will repair or replace software contained
within the products manufactured by Midmark (except for those not warranted under “Exclusions”) if: (1) the media on which the software is
furnished exhibits defects in material or workmanship under normal use; or (2) the software does not substantially conform to its published
speci cations.
APPLICABLE WARRANTY PERIOD The applicable warranty period, measured from the date of invoice to the original retail purchaser of
the product and shall be one (1) year for all warranted products and components.
OBTAINING WARRANTY SERVICE Warranty service must be obtained through either Midmark or an authorized dealer in the Midmark
product line for which warranty service is requested. Midmark may be contacted for warranty service inquiries or issues via email at www.
midmark.com; by phone at 1-800-MIDMARK or by mail to Midmark Corporation, 60 Vista Drive, Versailles, Ohio 45380. It is the retail purchaser’s obligation to arrange for delivery of a product to Midmark or one of its authorized dealers for warranty service, which delivery shall
be at retail purchaser’s expense. It is also the retail purchaser’s obligation to comply with the warranty service instructions provided either
by Midmark or its authorized dealer. The retail purchaser must provide Midmark with completed warranty registration information within
thirty (30) days after purchase in order to obtain the bene ts of this limited warranty.
EXCLUSIONS: This limited warranty does not cover and Midmark shall not be liable for the following:
(1) Defects, damage or other conditions caused, in whole or in part, by misuse, abuse, negligence, alteration, accident, freight damage,
negligent storage, tampering or failure to seek and obtain repair or replacement in a timely manner;
(2) Products which are not installed, used, and properly cleaned and maintained as required or recommended in the Midmark “Installation”
and/or “Installation/Operation Manual” for the applicable product, including the speci ed structural and operational environmental conditions
and electrical requirements;
(3) Products considered to be of a consumable or sterile nature;
(4) Accessories or parts not manufactured by Midmark;
(5) Charges by anyone for adjustments, repairs, replacement parts, installation or other work performed upon or in connection with such
products which are not expressly authorized in writing in advance by Midmark;
(6) Costs and expenses of routine maintenance and cleaning; and
(7) Representations and warranties made by any person or entity other than Midmark.
(8) Matching of color, grain or texture except to commercially acceptable standards;
(9) Changes in color caused by natural or arti cial light;
(10) Custom manufactured products;
(11) Alterations or modi cations to the product by any person or entity other than Midmark; and
(12) Products that would otherwise by covered under this limited warranty, but are acquired: (i) from a person or entity that is not Midmark
or one of its authorized dealers; or (ii) from a Midmark dealer that is not authorized to sell the product at issue in the geographic territory
where the purchaser is located, or is not authorized to sell the product at issue within the medical market.
SOFTWARE; WITH RESPECT TO SOFTWARE THAT IS A PRODUCT OR COMPONENT THEREOF, MIDMARK DOES NOT WARRANT
THAT THE SOFTWARE: (1) IS ERROR FREE; (2) CAN BE USED WITHOUT PROBLEMS OR INTERRUPTIONS; OR (3) IS FREE FROM
VULNERABILITY TO INTRUSION OR ATTACK BY VIRUSES OR OTHER METHODS.
EXCLUSIVE REMEDY; CONSEQUENTIAL DAMAGES DISCLAIMER MIDMARK’S ONLY OBLIGATION UNDER THIS LIMITED WARRANTY IS THE REPAIR OR REPLACEMENT OF DEFECTIVE PARTS. MIDMARK SHALL NOT BE LIABLE FOR AND HEREBY DISCLAIMS
ANY DIRECT, SPECIAL, INDIRECT, INCIDENTAL, EXEMPLARY OR CONSEQUENTIAL DAMAGES OR DELAYS, INCLUDING, BUT
NOT LIMITED TO, DAMAGES FOR LOSS OF PROFITS OR INCOME, LOSS OF USE, LOSS OF DATA, DOWNTIME, COVER AND
EMPLOYEE OR INDEPENDENT CONTRACTOR WAGES, PAYMENTS AND BENEFITS. THIS DISCLAIMER SHALL SURVIVE ANY
FAILURE OR ASSERTED FAILURE OF THE ESSENTIAL PURPOSE OF THIS LIMITED WARRANTY OR ITS REMEDIES SPECIFIED
HEREIN. WARRANTY DISCLAIMER THIS WARRANTY IS MIDMARK’S ONLY WARRANTY AND IS IN LIEU OF ALL OTHER WARRANTIES, EXPRESS OR IMPLIED. MIDMARK MAKES NO IMPLIED WARRANTIES OF ANY KIND INCLUDING ANY IMPLIED WARRANTIES
OF MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. THIS WARRANTY IS LIMITED TO THE REPAIR OR REPLACEMENT OF DEFECTIVE PARTS.
STATUTE OF LIMITATIONS No action may be brought against Midmark for breach of this limited warranty, an implied warranty, if any, or for
any other claim arising out of or relating to the products, more than ninety (90) days following expiration of the limited warranty period.
NO AUTHORIZATION No person or rm is authorized to create or approve for Midmark any other obligation or liability in connection with
the products.
Warranty Information
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