UMF Medical FUSIONONE 3001 User manual

SERIAL NUMBER
DATE OF MANUFACTURE
MAXIMUM PATIENT WEIGHT 500 LBS / 226 KG
UMFmedical.com
Ph: 814.266.8726 | Fax: [phone]
1316 Eisenhower Blvd. Johnstown, PA 15904
[email protected]
OWNER’S
MANUAL
FUSIONONE
POWER
EXAM CHAIR
3001/3002/3003
3-2518 Rev A

2
Safety First: This equipment must be operated and
maintained with the safety of the patient and doctor in mind.
1
No individual should operate table without reading and
understanding the owner’s manual. Read this manual
before operating your new UMF Medical equipment.
2Patients should only mount and dismount the table
from the front and only when the table is at a
comfortable height for their respective height.
3This product is intended to be used for positioning
of patients during medical examinations conducted
by qualied medical personnel.
4 This manual should remain permanently afxed
or near the equipment for convenient reference.
5Do not attempt to transport table without proper
lifting equipment.
Equipment Class — 3001 Class II, 3002 Class II, 3003 Class I

















CLASSIFICATIONS
APPLIED PARTS
IMPORTANT INFORMATION
6Do not leave table with unsupervised children.
7Use adhesive caution tape or cable runner if cord
is run across room.
8UMF Medical reserves the right to make changes
to the design of products at any time and without notice.
9If table becomes unresponsive while at a raised position with
a patient on the table, use a step stool, chair, or other form
of secure step to help the patient safely dismount the table.
10 Do not impede the table’s movement when raising or
lowering. Doing so can cause damage to table and or
item/person in contact with table.
11 Table can be lifted from the rear underside of the body panel
(under the drawer) and in the front by pulling out the leg section
approximately 4” and using it as a hand hold. Table should
always be lifted by two people at a time that are capable of
lifting 150lbs each. Table should be lifted onto a dolly or cart
capable of holding 300lbs for transporting long distances.
120VAC 9 AMP/220VAC 5 AMP 50-60HZ E514804
MEDICAL –GENERAL MEDICAL EQUIPMENT
AS TO ELECTRICAL SHOCK, FIRE AND MECHANICAL HAZARDS ONLY
IN ACCORDANCE WITH ANSI/AAMI ES60601-
1:A1:2012,C1:2009/®2012 AND A2:2010/®2012, CSA CAN/CSA-
C22.2 NO.60601-1:14, IEC 60601-1 EDITION 3.1 (2012), IEC 60601-
1-6:2010 (3RD EDITION) + A1:2013, IEC 62366: 2007 (1ST EDITION)
+ A1:2014
29ZE

3
TRANSPORT/STORAGE TEMPERATURE: -20ºC to 40ºC
TRANSPORT/STORAGE/OPERATING HUMIDITY: 95% maximum
OPERATING TEMPERATURE: 0ºC to 40ºC
1. This ME Equipment is intended for use in the professional healthcare setting.
2. WARNING: Use of this equipment adjacent to or stacked with other equipment should be
avoided because it could result in improper operation. If such use is necessary, this equipment
and the other equipment should be observed to verify that they are operating normally.
3. Maximum length of the power supply cable is not to exceed: 10 ft.
Maximum length of the hand/foot control cable is not to exceed: 10 ft.
4. WARNING: Use of accessories, transducers and cables other than those specied 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.
5. WARNING: 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 [ME EQUIPMENT or ME SYSTEM], including cables specied by the manufacturer.
Otherwise, degradation of the performance of this equipment could result.
6. There are no maintenance requirements specically related to EMC, all maintenance items
are addressed in the important information section
ENVIRONMENTAL CONDITIONS
SAFETY SYMBOLS
EMC INFORMATION
The warning symbol identies
special instructions or procedures,
which if not correctly followed
could result in personal injury.
WARNING: The caution symbol identies special
instructions or procedures, which if
not properly followed could result in
danger or damage to equipment.
CAUTION:
DO NOT STAND
DO NOT SIT
HOT SURFACE
GENERAL WARNING
REFER TO OWNER’S MANUAL
PROTECTIVE
EARTH GROUND
This product has been evaluated
with respect to electrical shock,
re, & mechanical hazards only,
in accordance with ANSI/AAMI
ES60601-1:A1:2012,C1:2009/
(R)2012 and A2:2010/(R)2012, CSA
CAN/CSA-C22.2 NO. 60601-1:14,
IEC 60601-1 Edition 3.1 (2012).
ATTENTION, CONSULT
ACCOMPANYING DOCUMENTS
TYPE B APPLIED PARTCLASS II EQUIPMENT

4
Enclosure Port
IMMUNITY TEST LEVELS
Phenomenon
Basic EMC standard
or test method
Professional healthcare
facility environment
Home healthcare
environment
Electrostatic discharge IEC 61000-4-2 ± 8 kV contact
± 2 kV, ± 4 kV, ± 8 kV, ± 15 kV air
Radiated RF EM elds a) IEC 61000-4-3
3 V/m f)
80 MHz – 2,7 GHz b)
80 % AM at 1 kHz c)
10 V/m f)
80 MHz – 2,7 GHz b)
80 % AM at 1 kHz c)
Proximity elds from RF
wireless communications
equipment
IEC 61000-4-3 See 8.10.
Rated power frequency
magnetic elds d) e) IEC 61000-4-8 30 A/m g)
50 Hz or 60 Hz
Input A.C. Power Port
IMMUNITY TEST LEVELS
Phenomenon
Basic EMC standard
or test method
Professional healthcare
facility environment Home healthcare environment
Electrical fast
transients / bursts a) l) o) IEC 61000-4-4 ± 2 kV
100 kHz repetition frequency
Surges a) b) j) o)
Line-to-line IEC 61000-4-5 ± 0,5 kV, ± 1 kV
Surges a) b) j) k) o)
Line-to-ground IEC 61000-4-5 ± 0,5 kV, ± 1 kV, ± 2 kV
Conducted
disturbances induced
by RF elds c) d) o)
IEC 61000-4-6
3 V m)
0,15 MHz – 80 MHz
6 V m) in ISM bands between 0,15 MHz
and 80 MHz n)
80 % AM at 1 kHze)
3 V m)
0,15 MHz – 80 MHz
6 V m) in ISM and amateur radio bands
between 0,15 MHz and 80 MHzn)
80 % AM at 1 kHz e)
Voltage dips f) p) r) IEC 61000-4-11
0 % UT; 0,5 cycleg)
At 0°, 45°, 90°, 135°, 180°, 225°, 270° and 315° q)
0 % UT; 1 cycle and
70 % UT; 25/30 cycles h)
Single phase: at 0°
Voltage interruptions
f) i) o) r) IEC 61000-4-11 0 % U ; 250/300 cycle h)
a) The interface between the PATIENT physiological signal simulation,
if used, and the ME EQUIPMENT or ME SYSTEM shall be located
within 0,1 m of the vertical plane of the uniform field area in one
orientation of the ME EQUIPMENT or ME SYSTEM.
b) ME EQUIPMENT and ME SYSTEMS that intentionally receive
RF electromagnetic energy for the purpose of their operation
shall be tested at the frequency of reception. Testing may be
performed at other modulation frequencies identified by the RISK
MANAGEMENT PROCESS. This test assesses the BASIC SAFETY
and ESSENTIAL PERFORMANCE of an intentional receiver when
an ambient signal is in the passband. It is understood that the
receiver might not achieve normal reception during the test.
c) Testing may be performed at other modulation frequencies
identified by the RISK MANAGEMENT PROCESS.
d) Applies only to ME EQUIPMENT and ME SYSTEMS with
magnetically sensitive components or circuitry.
e) During the test, the ME EQUIPMENT or ME SYSTEM may be
powered at any NOMINAL input voltage, but with the same
frequency as the test signal (see Table 1).
f) Before modulation is applied.
g) This test level assumes a minimum distance between the ME
EQUIPMENT or ME SYSTEM and sources of power frequency
magnetic field of at least 15 cm. If the RISK ANALYSIS shows
that the ME EQUIPMENT or ME SYSTEM will be used closer
than 15 cm to sources of power frequency magnetic field, the
IMMUNITY TEST LEVEL shall be adjusted as appropriate for
the minimum expected distance.
a) The test may be performed at any one power input voltage within
the ME EQUIPMENT or ME SYSTEM RATED voltage range. If
the ME EQUIPMENT or ME SYSTEM is tested at one power input
voltage, it is not necessary to re-test at additional voltages.
b) All ME EQUIPMENT and ME SYSTEM cables are attached during the test.
c) Calibration for current injection clamps shall be performed in a 150 Ω
system.

5
Test specicaons for Enclosure Port Immunity to RF wireless communicaons equipment
Test
frequency Band a) Service a) Modulaon b)
Maximum
power
Maximum
power
Immunity
Test Level
(MHz) (MHz) (W) (W) (V/m)
385 380 –390 TETRA 400 Pulse modulation b)
18 Hz 1,8 0,3 27
450 430 – 470 GMRS 460, FRS 460
FM c)
± 5 kHz deviation
1 kHz sine
2 0,3 28
710
704 – 787 LTE Band 13, 17 Pulse modulation b)
217 Hz 0,2 0,3 9745
780
810
800 – 960
GSM 800/900, TETRA
800, iDEN 820, CDMA
850, LTE Band 5
Pulse modulation b)
18 Hz 2 0,3 28870
930
1 720
1 700 –1 990
GSM 1800; CDMA 1900;
GSM 1900; DECT; LTE
Band 1, 3, 4, 25; UMTS
Pulse modulation b)
217 Hz 2 0,3 28
1 845
1 970
2 450 2 400 –2 570
Bluetooth, WLAN,
802.11 b/g/n, RFID 2450,
LTE Band 7
Pulse modulation b)
217 Hz 2 0,3 28
5 240
5 100 –5 800 WLAN 802.11 a/n Pulse modulation b)
217 Hz 0,2 0,3 95 500
5 785
d) If the frequency stepping skips over an ISM or amateur band,
as applicable, an additional test frequency shall be used in the
ISM or amateur radio band. This applies to each ISM and amateur
radio band within the specified frequency range.
e) Testing may be performed at other modulation frequencies
identified by the RISK MANAGEMENT PROCESS.
f) ME EQUIPMENT and ME SYSTEMS with a d.c. power input
intended for use with a.c.-to-d.c. converters shall be tested
using a converter that meets the specifications of the
MANUFACTURER of the ME EQUIPMENT or ME SYSTEM.
The IMMUNITY TEST LEVELS are applied to the a.c. power input
of the converter.
g) Applicable only to ME EQUIPMENT and ME SYSTEMS connected
to single-phase a.c. mains.
h) E.g. 10/12 means 10 periods at 50 Hz or 12 periods at 60 Hz.
i) ME EQUIPMENT and ME SYSTEMS with RATED input
current greater than 16 A / phase shall be interrupted once
for 250/300 cycles at any angle and at all phases at the same
time (if applicable). ME EQUIPMENT and ME SYSTEMS with
battery backup shall resume line power operation after the
test. For ME EQUIPMENT and ME SYSTEMS with RATED
input current not exceeding 16 A, all phases shall be interrupted
simultaneously.
j) ME EQUIPMENT and ME SYSTEMS that do not have a surge
protection device in the primary power circuit may be tested
only at ± 2 kV line(s) to earth and ± 1 kV line(s) to line(s).
k) Not applicable to CLASS II ME EQUIPMENT and ME SYSTEMS.
i) Direct coupling shall be used.
m) r.m.s., before modulation is applied.
n) The ISM (industrial, scientific and medical) bands between 0,15 MHz
and 80 MHz are 6,765 MHz to 6,795 MHz; 13,553 MHz to 13,567
MHz; 26,957 MHz to 27,283 MHz; and 40,66 MHz to 40,70 MHz. The
amateur radio bands between 0,15 MHz and 80 MHz are 1,8 MHz to 2,0
MHz, 3,5 MHz to 4,0 MHz, 5,3 MHz to 5,4 MHz, 7 MHz to 7,3 MHz,
10,1 MHz to 10,15 MHz, 14 MHz to 14,2 MHz, 18,07 MHz to 18,17
MHz, 21,0 MHz to 21,4 MHz, 24,89 MHz to 24,99 MHz, 28,0 MHz to 29,7
MHz and 50,0 MHz to 54,0 MHz.
o) Applicable to ME EQUIPMENT and ME SYSTEMS with RATED input
current less than or equal to 16 A / phase and ME EQUIPMENT and ME
SYSTEMS with RATED input current greater than 16 A / phase.
p) Applicable to ME EQUIPMENT and ME SYSTEMS with RATED input
current less than or equal to 16 A / phase.
q) At some phase angles, applying this test to ME EQUIPMENT with
transformer mains power input might cause an overcurrent protection
device to open. This can occur due to magnetic flux saturation of
the transformer core after the voltage dip. If this occurs, the ME
EQUIPMENT or ME SYSTEM shall provide BASIC SAFETY during and
after the test.
r) For ME EQUIPMENT and ME SYSTEMS that have multiple voltage
settings or auto ranging voltage capability, the test shall be performed at
the minimum and maximum RATED input voltage. ME EQUIPMENT and
ME SYSTEMS with a RATED input voltage range of less than 25 % of the
highest RATED input voltage shall be tested at one RATED input voltage
within the range. See Table 1 Note c) for examples calculations.
NOTE If necessary to achieve the IMMUNITY TEST LEVEL, the distance
between the transmitting antenna and the ME EQUIPMENT or ME
SYSTEM may be reduced to 1 m. The 1 m test distance is permitted by
IEC 61000-4-3.
a) For some services, only the uplink frequencies are included.
b) The carrier shall be modulated using a 50 % duty cycle
square wave signal.
c) As an alternative to FM modulation, 50 % pulse modulation
at 18 Hz may be used because while it does not represent
actual modulation, it would be worst case.

6
Maximum Patient Weight 500 lbs (226 kg)
Electrical Supply(Standard) 120V 50-60HZ 9AMP
Electrical Supply(Optional) 220V 50-60HZ 5AMP
Power Cord Length 10 FT (3.0m)
Table Weight 400 lbs (181kg)
Paper Roll (Maximum size) 21.0” Long x 3.5” Diameter
(53.3 cm x 8.9 cm)
Storage Drawer (Front) 19.0” W x 12.0” D x 3.5” H
(48 cm x 30 cm x 9 cm)
Storage Drawer (Side) 24.5” W x 12.5” D x 3.5” H
(62 cm x 32 cm x 9 cm)
SPECIFICATIONS

7
Backrest Adjustment (Manual Operaon)
1Depress release handle.
2Adjust backrest to desired position.
3Release handle to lock.



WARNING:
Hand & Foot Control — Table Operaon
FEATURES AND OPERATION
Hand Control Foot Control
Table High/Low Funcon Operaon:
1Press the up button to raise the table
2Press the down button to lower the table


WARNING:
Oponal (accessory — 581)

8
Side Drawer
21” x 17.5” x 5”
(53cm x 44cm x 13cm)
Front Drawer
18” x 12.0” x 3”
(46cm x 30cm x 8cm)
Storage Drawers
Drip Pan
Leg Rest
1Slide the drain pan drawer out to access drain pan.
2Push drain pan drawer back in when not in use.
3Drain pan can lift out of the drawer for cleaning purposes.
1Slide leg section forward until it contacts the two
stopper pins.
2When not in use, push the leg section in to stow.
3Leg rest capacity should not exceed 100lbs.


WARNING:


WARNING:
FEATURES AND OPERATION
Products placed in warming drawer should be checked for proper temperature before use.
Maximum weight for each drawer is not to exceed 10lbs.

9
Max Roll Size
21” x 3.5” (53cm x 9cm)
Paper Roll Replacement
Srrup Posioning & Adjustment
Pelvic Tilt
Slide rod out of brackets, install new
roll, and reinstall into brackets
1Pull the stirrups out and unfold.
2Lift slightly and move left or right to position.
3Release stirrup to lock into position.
1Lift up the seat and the pelvic tilt rod will
automatically fall into place.
2 To disengage pelvic tilt, lift seat and ip the
lever on either side of the seat back.
ENSURE PELVIC SUPPORT ARM IS LOCKED
AND HANDS ARE NOT UNDERNEATH BUMPER
WHEN LOWERING SEAT SECTION.




WARNING:
FEATURES AND OPERATION

10
FEATURES AND OPERATION
Reversing Side Drawers
Step 1:
Remove side panels.
Step 3:
Slide cages to opposite
side of table.
Step 5:
Install side panel on
opposite side.
Step 2:
Remove drawer
› Extend drawer
› Press tabs on both sides
› Remove drawer
Step 4:
Align slides and install
drawer on opposite side.
* Slide in until an audible
“click!” is heard.

11
Drawer Warmer
1Press switch to power on and off.
2When switch is in it’s on position switch will
illuminate indicating drawer warmer is activated.
3During normal operation, the front drawer and its
contents should be between 100°F and 110°F. If
temperatures exceed 120°F contact UMF Medical
Customer Service.
COMMON OPTIONS AND ACCESSORIES





WARNING:

12
COMMON OPTIONS AND ACCESSORIES
Hospital Grade Receptacle










WARNING:


WARNING:
WARNING:



WARNING:
Service Note: If the maximum load of the receptacle is exceeded, two circuit breakers will interrupt power. To reset, toggle the far two
circuit breakers located behind the receptacle outlet box in the back of the drawer panel.

13
COMMON OPTIONS AND ACCESSORIES
Bierho Knee Crutch (251-Pair)
1Extend stirrups to full-extended position
with heel stirrup in retracted position.
2Insert knurled end of knee crutch rod into
hole on end of stirrup.
3Adjust to position and tighten with slide lock.

14
CABLE CONNECTION
Plug Power Cable into Column
Flip Cable Lock Down
Plug Control Cable Into column
Note: Make sure to posion table such that the access to the cable connecon is not impeded under normal use.

15
Plug Power Supply Into Wall
1This is an image of the table’s power supply. When
plugged in, the indicator light should be illuminated
indicating the power supply is operating correctly
Note: The table does not have an on/o switch so
whenever the power supply is plugged in and connected
to the column, the table is operable.

16
EQUIPMENT CARE

The upholstery material used on the top, leg rest, an
headrest is resistant to most medical stains.
For light cleaning:
1
A solution of 10% liquid soap and clean water applied with a
soft damp cloth will remove disinfection cleaner build-up.
2
If necessary, a solution of liquid cleanser and water can be
applied with a soft bristle brush. Wipe away residue with a
water-dampened cloth.

1
Dampen a soft white cloth with a solution of standard bleach
(sodium hypochlorite) or other chlorine-based cleaner***
and water; 10% bleach, 90% water.
2
Rub gently.
3If necessary, allow the 1:10 diluted bleach (sodium
hypochlorite) solution to puddle on the affected area or
apply with a clean, soaked cloth for approximately 30
minutes. Rinse with a water-dampened cloth to remove
any remaining bleach concentration.
4
Rinse with a water-dampened cloth to remove cleaner
solution and allow thorough drying of material.
***See current CDC Guideline for Disinfecon & Sterilizaon in
Healthcare Facilies for bleach alternave cleaners.
In laboratory testing, upholstery
protected with PreFixx
®
nish
was treated with the following
disinfectants with little to no
discoloration or damage to the
upholstery. This testing may not
reect actual results in the eld.*

› Clorox
®
Broad Spectrum Quaternary
Disinfectant Cleaner
› Clorox
®
Healthcare Bleach
Germicidal Cleaner
›Clorox
®
Healthcare Bleach
Germicidal Wipes
› Clorox
®
Healthcare EZ-KILL
®
Wipes





CAUTION:
Proper Sterilizaon Instrucons
Upholstery with PreFixx®
Protecve Finish
›Clorox®Healthcare VersaSure®
Cleaner Disinfection Wipes
›Clorox®Hydrogen Peroxide
Cleaner Disinfectant Spray
›Clorox®Hydrogen Peroxide
Cleaner Disinfectant Wipes
›Agar™ Powerquat
›Asepticare™
›Asepticare™ TB-II
›AVISTAT-D™ Ready To Use
Spray Disinfectant Cleaner
›Biotrol BirexSE®
›Bleach 1:5 (20% bleach)
›Bleach 1:9 (10% bleach)
›Bleach-Rite® Disinfecting Spray
›CaviCide™
›CaviCide1™
›CaviCide™ AF
Note: Immediately remove any uid spilled on upholstery surface.
Antimicrobial: UMF Medical Upholstery providers outstanding
protection in difcult medical and healthcare environments and
contains an agent effective against bacterial and fungal microorganisms.

A chemical acid-resistant paint is used, but extreme care must be
taken not to use ammonia-based cleaners or discoloration of paint may
occur. A damp cloth or mild liquid soap solution should be sufcient.

All non-painted surfaces, chrome plated, or stainless steel should be
wiped weekly with a clean damp cloth then buffed to a lustrous shine
with a soft dry cloth.

The protective base is easily washable with mild liquid soap and water.
A soft bristle brush may be used on scuffed stained areas.
›Diversey™ Accel®
INTERVention®Wipes
›Diversey™ Avert®Sporicidal
Disinfectant Cleaner
›ERC Performance Wipes
›McKesson Disposable
Germicidal Surface Wipes
›McKesson Pro-Tech RTU
Disinfectant Cleaner
›OPTIM®1 Wipes
›OPTIM®33TB
›Oxivir®1 RTU
›Oxivir®Five 16
›Oxivir®TB
›OxyCide™ Daily
Disinfectant Cleaner
›PDI Sani-Cloth®AF3
Germicidal Disposable Wipes

17
QUESTIONS, COMMENTS OR SERVICE REQUESTS
DISPOSAL INFORMATION

UMF Medical Customer Service
1316 Eisenhower Blvd
Johnstown, PA 15904
1When disposing of your equipment, there are no batteries, harmful
chemicals, or other potentially hazardous items contained within
the equipment that require any special disposal precautions.
2Metal, plastic, and other components of table can be disassembled
and recycled if desired.
Toll Free: 1(800) 638-5322
Email: [email protected]
Fax: [phone]
* For service requests, please have model % serial number available.
EQUIPMENT CARE
›PDI Sani-Cloth®HB
›PDI Sani-Cloth®Plus
›PDI Sani-Cloth®Prime
Germicidal Disposable Wipe
›PDI Super Sani-Cloth®
›PDI Super Sani-Cloth®Bleach
Germicidal Disposable Wipes
›Precise QTB Spray
›PROCHEM®Oxy Plus
›
Purell
®
Healthcare Surface Disinfectant
›Purell®Multi-Surface Disinfectant
›Sani Professional®Cleaning +
Degreasing Multi-Surface Wipes
›Sani Professional®Multi-Surface
Cleaning Wipes
›Sani Professional®No-Rinse
Sanitizing Multi-Surface Wipes
›SaniZide®Plus
› STERI-7 XTRA CONCENTRATE
(recommended dilution ratio 1:10)
› STERI-7 XTRA WIPES
›Vert-2-Go ED
›Virox AHP 5
›Virox PREempt™ RTU
›Virex®II 256
›Virex®Plus One-Step
Disinfectant Cleaner & Deodorant
›Wayne®Concept 256N
›Wex-Cide 128

Use one of the following cleaners
with a soft cloth
or damp sponge.
Rinse area
with fresh water then
dry with a clean, lint-free cloth.
Primary Recommended Cleaner
›Formula 409 All-
Purpose spray cleaner
›Fantastik spray cleaner
Secondary
Recommended Cleaners
›Lysol Clean and Fresh
Multi-Surface Cleaner
(Reckitt Benckiser)
›Lestoil Heavy Duty
Cleaner (Clorox)
›Mr. Clean / Flash
Clean and Shine
(Procter and Gamble)
›Eco Touch All Purpose
Premium Care
For more difcult stains, contact
UMF Medical Customer Service.
*All disinfectants and cleaning agents
contain chemicals that degrade coated
fabric upholstery to some extent. To promote
a long product life, it is recommended that
the PreFixx cleaning and maintenance
protocol be employed regularly.
**Inclusion in this document does not
imply “t for use.”
Customers should rst
determine if products are appropriate
for
use on their surfaces.

18
WARRANTY INFORMATION

UMF Medical warrants to the original purchaser a warranty
for products to be free from functional defects in material
and workmanship under normal interior use and service. UMF
Medical’s obligation under this warranty is limited to the
repair or replacement, at UMF Medical’s option, of the parts
or the products the defects of which are reported to UMF
Medical within the applicable warranty period and which upon
examination by UMF Medical prove to be defective. Warranty
subject to the terms and conditions listed below.
Length of warranty, measured by Purchase Date (Invoice Date),
for all warranted products and components:
Five years: Signature Series Examination Tables
(52xx model numbers and Treatment and
Orthopedic Tables (55xx model numbers).
Ultra-Comfort adjustable backrest cylinder
not included.
Three years: Power Exam and Procedure Tables and all
other UMF Medical products excluding the
products listed in Five Year and One Year
categories of this document.
One year: Waste Receptacles, Bassinet Baskets,
Bassinet Mattresses and ultra-comfort
adjustable backrest cylinder.

Warranty service must be obtained by contacting either
the Authorized Distributor through whom the product was
purchased or UMF Medical Customer Service Department via
phone at 814-266-8726, or via email at customerservice@
umfmedical.com.
This warranty covers the cost associated with the repair parts
only and does not cover any other charges, including but not
limited to service calls, labor, transportation, shipping, etc.
It is the retail customer’s obligation to arrange delivery of a
product to UMF Medical or one of its authorized distributors
for warranty service, which delivery shall be at the retail
purchaser’s expense. It is also the retail purchaser’s obligation
to comply with the warranty service instruction provided by
UMF Medical or its authorized distributor. The retail purchaser
must provide UMF Medical with completed warranty registration
information within thirty days after purchase in order to obtain
the benets of this warranty.
Limited warranty general excepons and exclusions
This warranty does not cover and UMF Medical shall not be
liable for the following:
› Parts and products of a consumable nature;
› Defects, damage or other conditions caused, in whole or in
part, by mishandling, misuse, abuse, negligence, alteration,
accident, freight damage, tampering or failure to seek
and obtain repair or replacement in a timely manner;
›
Products which are not installed, used, and properly cleaned
and maintained as required in the UMF Medical installation
and/or Owner’s Manual for the applicable product;
› Replacement parts, alterations or installation of any
accessories or parts not manufactured or recommended
by UMF Medical;
› Cosmetic and non-functional defects not noted at time
of delivery.
› Charges for repairs, replacement parts, adjustments,
installation or other work performed upon or in connection
with products which are not expressly authorized in writing
in advance by UMF Medical.
›
Damages resulting from inadequate power supply (including
incorrect voltage, voltage spikes or other irregularities) or
use or storage in corrosive atmospheres.
To the extent any or all of the following exclusions or
provisions of this warranty are prohibited by any federal, state,
or municipal law which cannot be preempted, those exclusions
or provisions shall not be applicable.
Exclusive Remedy: Consequenal Damages Disclaimer
UMF Medical’s only obligation under this warranty is the repair
or replacement of defective parts. UMF Medical 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 prots or
income, loss of use, downtime, employee or independent
contractor wages, payments and benets, commercial loss
or other incidental charges.
No Authorizaon
No person or firm is authorized to create or approve for
UMF Medical any other obligation or liability in connection
with the products.
Warranty Disclaimer
THIS WARRANTY IS UMF MEDICAL’S ONLY WARRANTY
AND IS IN LIEU OF ALL OTHER WARRANTIES, EXPRESS OR
IMPLIED. UMF MEDICAL MAKES NO IMPLIED WARRANTIES
OF ANY KIND INCLUDING ANY IMPLIED WARRANTIES
OR MERCHANTABILITY OR FITNESS FOR A PARTICULAR
PURPOSE. THIS WARRANTY IS LIMITED TO THE REPAIR OR
REPLACEMENT OF DEFECTIVE PARTS.
No action may be brought against UMF Medical for breach
of this limited warranty, an implied warranty, if any, or for any
other claim arising out of or relating to the products following
expiration of the limited warranty period.
UMF Medical reserves the right to make changes in the design
or material of its products without incurring any obligation
to incorporate such changes in any product previously
manufactured.

19
This page intentionally left blank

UMFmedical.com
Ph: 814.266.8726 | Fax: [phone]
1316 Eisenhower Blvd. Johnstown, PA 15904
[email protected]