OWNER’S

MANUAL
FUSIONONE
POWER
EXAM CHAIR
3001/3002/3003

SERIAL NUMBER

DATE OF MANUFACTURE

MAXIMUM PATIENT WEIGHT 500 LBS / 226 KG

Ph: 814.266.8726 | Fax: 814.266.1870

1316 Eisenhower Blvd. Johnstown, PA 15904 UMFmedical.com
[email protected] Revision B
IMPORTANT INFORMATION
6 Do not leave table with unsupervised children.
Safety First: This equipment must be operated and
maintained with the safety of the patient and doctor in mind. 7 Use adhesive caution tape or cable runner if cord
is run across room.
1 No individual should operate table without reading and 8 UMF Medical reserves the right to make changes
understanding the owner’s manual. Read this manual to the design of products at any time and without notice.
before operating your new UMF Medical equipment. 9 If table becomes unresponsive while at a raised position with
2 Patients should only mount and dismount the table a patient on the table, use a step stool, chair, or other form
from the front and only when the table is at a of secure step to help the patient safely dismount the table.
comfortable height for their respective height. 10 Do not impede the table’s movement when raising or
This product is intended to be used for positioning lowering. Doing so can cause damage to table and or
3
of patients during medical examinations conducted item/person in contact with table.
by qualified medical personnel. 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
4 This manual should remain permanently affixed
approximately 4” and using it as a hand hold. Table should
or near the equipment for convenient reference.
always be lifted by two people at a time that are capable of
5 Do not attempt to transport table without proper lifting 150lbs each. Table should be lifted onto a dolly or cart
lifting equipment. capable of holding 300lbs for transporting long distances.

CLASSIFICATIONS
Equipment Class — 3001 Class II, 3002 Class II, 3003 Class I
Protection against electric shock: Type B applied parts
Protection against harmful ingress of water: Ordinary Equipment
is not suitable for use in the presence of a flammable anesthetics 29ZE 120VAC 9 AMP/220VAC 5 AMP 50-60HZ E514804
mixture with air or with oxygen or with nitrous oxide MEDICAL – GENERAL MEDICAL EQUIPMENT
AS TO ELECTRICAL SHOCK, FIRE AND MECHANICAL HAZARDS ONLY
Mode of Operation: Continuous operation with intermittent loading IN ACCORDANCE WITH ANSI/AAMI ES60601-
1 minute on 9 minutes off or 2 minutes on, 18 minutes off. 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-
The table, any manufacturer approved accessories, and all 1-6:2010 (3RD EDITION) + A1:2013, IEC 62366: 2007 (1ST EDITION)
accompanying documents are all part of the Medical Equipment + A1:2014

System and suitable for use within the patient environment.

This product has been evaluated with respect to electrical shock,
fire, & 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).

APPLIED PARTS
The entire table is considered to be an applied part because the patient or
practitioner could come in contact with any part of the table while in use.
It is noted that the only components designed to come in contact with the
patient on a regular occurrence are the upholstered top, leg pad, and stirrups.

2
SAFETY SYMBOLS

WARNING: The warning symbol identifies CAUTION: The caution symbol identifies special
special instructions or procedures, instructions or procedures, which if
which if not correctly followed not properly followed could result in
could result in personal injury. danger or damage to equipment.

This product has been evaluated

with respect to electrical shock,
CLASS II EQUIPMENT TYPE B APPLIED PART
fire, & mechanical hazards only,
in accordance with ANSI/AAMI
ES60601-1:A1:2012,C1:2009/
(R)2012 and A2:2010/(R)2012, CSA
ATTENTION, CONSULT PROTECTIVE
CAN/CSA-C22.2 NO. 60601-1:14,
ACCOMPANYING DOCUMENTS EARTH GROUND
IEC 60601-1 Edition 3.1 (2012).

REFER TO OWNER’S MANUAL GENERAL WARNING HOT SURFACE

DO NOT SIT DO NOT STAND

ENVIRONMENTAL CONDITIONS
TRANSPORT/STORAGE TEMPERATURE: -20ºC to 40ºC
TRANSPORT/STORAGE/OPERATING HUMIDITY: 95% maximum
OPERATING TEMPERATURE: 0ºC to 40ºC

EMC INFORMATION
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 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.
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 specified by the manufacturer.
Otherwise, degradation of the performance of this equipment could result.
6. There are no maintenance requirements specifically related to EMC, all maintenance items
are addressed in the important information section

3
Enclosure Port
IMMUNITY TEST LEVELS

Basic EMC standard Professional healthcare Home healthcare

Phenomenon or test method facility environment environment
± 8 kV contact
Electrostatic discharge IEC 61000-4-2
± 2 kV, ± 4 kV, ± 8 kV, ± 15 kV air
3 V/m f) 10 V/m f)
Radiated RF EM fields a)
IEC 61000-4-3 80 MHz – 2,7 GHz b) 80 MHz – 2,7 GHz b)
80 % AM at 1 kHz c) 80 % AM at 1 kHz c)
Proximity fields from RF
wireless communications IEC 61000-4-3 See 8.10.
equipment
Rated power frequency 30 A/m g)
IEC 61000-4-8
magnetic fields d) e) 50 Hz or 60 Hz

a) The interface between the PATIENT physiological signal d) Applies only to ME EQUIPMENT and ME SYSTEMS with
simulation, if used, and the ME EQUIPMENT or ME SYSTEM shall magnetically sensitive components or circuitry.
be located within 0,1 m of the vertical plane of the uniform field e) During the test, the ME EQUIPMENT or ME SYSTEM may be
area in one orientation of the ME EQUIPMENT or ME SYSTEM. powered at any NOMINAL input voltage, but with the same
b) ME EQUIPMENT and ME SYSTEMS that intentionally receive frequency as the test signal (see Table 1).
RF electromagnetic energy for the purpose of their operation f) Before modulation is applied.
shall be tested at the frequency of reception. Testing may be
performed at other modulation frequencies identified by the RISK g) This test level assumes a minimum distance between the ME
MANAGEMENT PROCESS. This test assesses the BASIC SAFETY EQUIPMENT or ME SYSTEM and sources of power frequency
and ESSENTIAL PERFORMANCE of an intentional receiver when magnetic field of at least 15 cm. If the RISK ANALYSIS
an ambient signal is in the passband. It is understood that the shows that the ME EQUIPMENT or ME SYSTEM will be used
receiver might not achieve normal reception during the test. closer than 15 cm to sources of power frequency magnetic
field, the IMMUNITY TEST LEVEL shall be adjusted as
c) Testing may be performed at other modulation frequencies appropriate for the minimum expected distance.
identified by the RISK MANAGEMENT PROCESS.

Input A.C. Power Port

IMMUNITY TEST LEVELS

Basic EMC standard Professional healthcare

Home healthcare environment
Phenomenon or test method facility environment
Electrical fast ± 2 kV
IEC 61000-4-4
transients / bursts a) l) o) 100 kHz repetition frequency
Surges a) b) j) o)
IEC 61000-4-5 ± 0,5 kV, ± 1 kV
Line-to-line
Surges a) b) j) k) o)
IEC 61000-4-5 ± 0,5 kV, ± 1 kV, ± 2 kV
Line-to-ground
3 V m) 3 V m)
Conducted 0,15 MHz – 80 MHz 0,15 MHz – 80 MHz
disturbances induced IEC 61000-4-6 6 V m) in ISM bands between 0,15 6 V m) in ISM and amateur radio bands
by RF fields c) d) o) MHz and 80 MHz n) between 0,15 MHz and 80 MHz n)
80 % AM at 1 kHz e) 80 % AM at 1 kHz e)
0 % UT ; 0,5 cycle g)
At 0°, 45°, 90°, 135°, 180°, 225°, 270° and 315° q)
Voltage dips f) p) r) IEC 61000-4-11 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 test may be performed at any one power input voltage within b) All ME EQUIPMENT and ME SYSTEM cables are attached during the test.
the ME EQUIPMENT or ME SYSTEM RATED voltage range. If c) Calibration for current injection clamps shall be performed in a 150 Ω
the ME EQUIPMENT or ME SYSTEM is tested at one power input system.
voltage, it is not necessary to re-test at additional voltages. 4
 d) If the frequency stepping skips over an ISM or amateur band, i) Direct coupling shall be used.
as applicable, an additional test frequency shall be used in the m) r.m.s., before modulation is applied.
ISM or amateur radio band. This applies to each ISM and amateur
radio band within the specified frequency range. 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
e) Testing may be performed at other modulation frequencies MHz; 26,957 MHz to 27,283 MHz; and 40,66 MHz to 40,70 MHz.
identified by the RISK MANAGEMENT PROCESS. The amateur radio bands between 0,15 MHz and 80 MHz are 1,8 MHz
f) ME EQUIPMENT and ME SYSTEMS with a d.c. power input to 2,0 MHz, 3,5 MHz to 4,0 MHz, 5,3 MHz to 5,4 MHz, 7 MHz to
intended for use with a.c.-to-d.c. converters shall be tested 7,3 MHz, 10,1 MHz to 10,15 MHz, 14 MHz to 14,2 MHz, 18,07 MHz
using a converter that meets the specifications of the to 18,17 MHz, 21,0 MHz to 21,4 MHz, 24,89 MHz to 24,99 MHz, 28,0
MANUFACTURER of the ME EQUIPMENT or ME SYSTEM. MHz to 29,7 MHz and 50,0 MHz to 54,0 MHz.
The IMMUNITY TEST LEVELS are applied to the a.c. power input o) Applicable to ME EQUIPMENT and ME SYSTEMS with RATED input
of the converter. current less than or equal to 16 A / phase and ME EQUIPMENT and ME
g) Applicable only to ME EQUIPMENT and ME SYSTEMS SYSTEMS with RATED input current greater than 16 A / phase.
connected to single-phase a.c. mains. p) Applicable to ME EQUIPMENT and ME SYSTEMS with RATED input
h) E.g. 10/12 means 10 periods at 50 Hz or 12 periods at 60 Hz. current less than or equal to 16 A / phase.
i) ME EQUIPMENT and ME SYSTEMS with RATED input q) At some phase angles, applying this test to ME EQUIPMENT with
current greater than 16 A / phase shall be interrupted once transformer mains power input might cause an overcurrent protection
for 250/300 cycles at any angle and at all phases at the same device to open. This can occur due to magnetic flux saturation of
time (if applicable). ME EQUIPMENT and ME SYSTEMS with the transformer core after the voltage dip. If this occurs, the ME
battery backup shall resume line power operation after the EQUIPMENT or ME SYSTEM shall provide BASIC SAFETY during and
test. For ME EQUIPMENT and ME SYSTEMS with RATED after the test.
input current not exceeding 16 A, all phases shall be interrupted r) For ME EQUIPMENT and ME SYSTEMS that have multiple voltage
simultaneously. settings or auto ranging voltage capability, the test shall be performed at
j) ME EQUIPMENT and ME SYSTEMS that do not have a surge the minimum and maximum RATED input voltage. ME EQUIPMENT and
protection device in the primary power circuit may be tested ME SYSTEMS with a RATED input voltage range of less than 25 % of the
only at ± 2 kV line(s) to earth and ± 1 kV line(s) to line(s). highest RATED input voltage shall be tested at one RATED input voltage
k) Not applicable to CLASS II ME EQUIPMENT and ME SYSTEMS. within the range. See Table 1 Note c) for examples calculations.

Test specifications for Enclosure Port Immunity to RF wireless communications equipment

Test Maximum Maximum Immunity
frequency Band a) Service a) Modulation b) power power Test Level
(MHz) (MHz) (W) (W) (V/m)

Pulse modulation b)
385 380 –390 TETRA 400 1,8 0,3 27
18 Hz
FM c)
450 430 – 470 GMRS 460, FRS 460 ± 5 kHz deviation 2 0,3 28
1 kHz sine
710
Pulse modulation b)
745 704 – 787 LTE Band 13, 17 0,2 0,3 9
217 Hz
780
810
GSM 800/900, TETRA
Pulse modulation b)
870 800 – 960 800, iDEN 820, CDMA 2 0,3 28
18 Hz
850, LTE Band 5
930
1 720
GSM 1800; CDMA 1900;
Pulse modulation b)
1 845 1 700 –1 990 GSM 1900; DECT; LTE 2 0,3 28
217 Hz
Band 1, 3, 4, 25; UMTS
1 970
Bluetooth, WLAN,
Pulse modulation b)
2 450 2 400 –2 570 802.11 b/g/n, RFID 2 0,3 28
217 Hz
2450, LTE Band 7
5 240
Pulse modulation b)
5 500 5 100 –5 800 WLAN 802.11 a/n 0,2 0,3 9
217 Hz
5 785

NOTE If necessary to achieve the IMMUNITY TEST LEVEL, the distance a) For some services, only the uplink frequencies are included.
between the transmitting antenna and the ME EQUIPMENT or ME b) The carrier shall be modulated using a 50 % duty cycle
SYSTEM may be reduced to 1 m. The 1 m test distance is permitted by square wave signal.
IEC 61000-4-3.
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. 5
SPECIFICATIONS

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)

21.0” Long x 3.5” Diameter
Paper Roll (Maximum size)
(53.3 cm x 8.9 cm)
19.0” W x 12.0” D x 3.5” H
Storage Drawer (Front)
(48 cm x 30 cm x 9 cm)
24.5” W x 12.5” D x 3.5” H
Storage Drawer (Side)
(62 cm x 32 cm x 9 cm)

6
FEATURES AND OPERATION

Hand & Foot Control — Table Operation

Hand Control Foot Control

Optional (accessory — 581)

Table High/Low Function Operation:

1 Press the up button to raise the table
2 Press the down button to lower the table

WARNING: DO NOT PLACE FOOT REST

ON BASE DURING OPERATION

Backrest Adjustment (Manual Operation)

1 Depress release handle.
2 Adjust backrest to desired position.
3 Release handle to lock.

WARNING: DO NOT USE BACKREST AS A SEAT.

BACKREST IS NOT DESIGNED TO
SUPPORT PATIENT’S FULL WEIGHT

7
FEATURES AND OPERATION

Storage Drawers

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)

Products placed in warming drawer should be checked for proper temperature before use.
Maximum weight for each drawer is not to exceed 10lbs.

Drain Pan

1 Slide the drain pan drawer out to access drain pan.

2 Push drain pan drawer back in when not in use.
3 Drain pan can lift out of the drawer for cleaning purposes.

WARNING: DO NOT USE DRAWER OR DRAIN PAN

AS A SEAT OR STEP.

Leg Rest

1 Slide leg section forward until it contacts the two

stopper pins.
2 When not in use, push the leg section in to stow.
3 Leg rest capacity should not exceed 100lbs.

WARNING: DO NOT USE THE LEG REST AS A

SEAT OR STEP.

8
FEATURES AND OPERATION

Paper Roll Replacement

Max Roll Size

21” x 3.5” (53cm x 9cm)

Slide rod out of brackets, install new

roll, and reinstall into brackets

Stirrup Positioning & Adjustment

1 Pull the stirrups out and unfold.

2 Lift slightly and move left or right to position.
3 Release stirrup to lock into position.

WARNING: DO NOT SUPPORT THE PATIENT’S ENTIRE

WEIGHT WITH THE STIRRUPS. ENSURE
STIRRUPS ARE PROPERLY LOCKED PRIOR
TO ENGAGING PATIENTS FEET.

Pelvic Tilt

1 Lift up the seat and the pelvic tilt rod will

automatically fall into place.
2 To disengage pelvic tilt, lift seat and flip 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.

9
FEATURES AND OPERATION

Reversing Side Drawers

Step 1: Step 3:

Remove side panel Slide cages to opposite

with a screwdriver. side of table.

Step 4:
Align slides and install
drawer on opposite side.
Step 2:
› Ensure slide cages are
Remove drawer to the front of the track
› Extend drawer › Align both drawer tracks
› Slide both tabs, with the slide cages
located in the track › Slide drawer in
under the drawer, to completely
the side and hold
› Remove drawer Step 5:
Install side panel on
opposite side with a
screwdriver.

10
COMMON OPTIONS AND ACCESSORIES

Drawer Warmer

1 Press switch to power on and off.

2 When switch is in it’s on position switch will
illuminate indicating drawer warmer is activated.
3 During 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.

WARNING: THE HEATING ELEMENT FOR THE

DRAWER WARMER IS LOCATED IN A
PANEL ABOVE THE DRAWER, THIS PANEL
WILL BE HOT WHILE DRAWER WARMER
IS ON AND IS NOT TO BE TOUCHED.

11
COMMON OPTIONS AND ACCESSORIES

Hospital Grade Receptacle

WARNING: OUTLET IS FOR MEDICAL EQUIPMENT ONLY.

CAUTION: CHECK GROUND CONTINUITY PERIODICALLY.
120V MAXIMUM OUTPUT - 5.0A, 120V
220V MAXIMUM OUTPUT - 2.5A, 220V

WARNING: DO NOT DISCARD COVER. COVER IS TO BE REAPPLIED AFTER REMOVAL OF EQUIPMENT FROM
MULTIPLE SOCKET OUTLET.

WARNING: MULTIPLE SOCKET OUTLET LOCATED ON SIDE OF TABLE IS TO BE USED FOR MEDICAL EQUIPMENT ONLY
(WHERE SAFETY CERTIFICATION HAS BEEN PERFORMED IN ACCORDANCE TO IEC 60601-1 AND/OR IEC
60601-1-1). USE OF EQUIPMENT NOT COMPLYING WITH THE EQUIVALENT SAFETY REQUIREMENT OF THIS
EQUIPMENT MAY LEAD TO A REDUCED LEVEL OF SAFETY OF THE RESULTING SYSTEM. THE MULTIPLE SOCKET
OUTLET LOCATED ON THE BACK SIDE OF THE PANEL, ON THE INSIDED OF THE TABLE, IS TO BE USED FOR
THE POWER SUPPLY FOR THE COLUMN ONLY, THIS OUTLET SHOULD NOT BE USED FOR ANY OTHER ITEMS.

WARNING: GROUND RELIABILITY CAN ONLY BE ACHIEVED WHEN POWER SUPPLY IS CONNECTED TO AN EQUIVALENT
RECEPTACLE MARKED “HOSPITAL ONLY” OR “HOSPITAL GRADE”. WARNING: ADDITIONAL EXTENSION CORD OR
MULTI-SOCKET OUTLET IS NOT TO BE CONNECTED TO TABLE.

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.

12
COMMON OPTIONS AND ACCESSORIES

Bierhoff Knee Crutch (251-Pair)

1 Extend stirrups to full-extended position

with heel stirrup in retracted position.
2 Insert knurled end of knee crutch rod into
hole on end of stirrup.
3 Adjust to position and tighten with slide lock.

13
CABLE CONNECTION

Plug Power Cable into Column

Flip Cable Lock Down

Plug Control Cable Into column

Note: Make sure to position table such that the access to the cable connection is not impeded under normal use.

14
Plug Power Supply Into Wall

1 This 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/off switch so

whenever the power supply is plugged in and connected
to the column, the table is operable.

15
EQUIPMENT CARE

Proper Sterilization Instructions

Care of upholstery Note: Immediately remove any fluid spilled on upholstery surface.
The upholstery material used on the top, leg rest, an
headrest is resistant to most medical stains. Antimicrobial: UMF Medical Upholstery providers outstanding
protection in difficult medical and healthcare environments and
For light cleaning: contains an agent effective against bacterial and fungal microorganisms.

1 A solution of 10% liquid soap and clean water applied with a

Care of painted surfaces
soft damp cloth will remove disinfection cleaner build-up.
If necessary, a solution of liquid cleanser and water can be A chemical acid-resistant paint is used, but extreme care must be
2
applied with a soft bristle brush. Wipe away residue with a taken not to use ammonia-based cleaners or discoloration of paint may
water-dampened cloth. occur. A damp cloth or mild liquid soap solution should be sufficient.

For disinfection: Care of bright metal surfaces

1 Dampen a soft white cloth with a solution of standard bleach All non-painted surfaces, chrome plated, or stainless steel should be
(sodium hypochlorite) or other chlorine-based cleaner*** wiped weekly with a clean damp cloth then buffed to a lustrous shine
and water; 10% bleach, 90% water. with a soft dry cloth.
2 Rub gently.
3 If necessary, allow the 1:10 diluted bleach (sodium Care of base
hypochlorite) solution to puddle on the affected area or The protective base is easily washable with mild liquid soap and water.
apply with a clean, soaked cloth for approximately 30 A soft bristle brush may be used on scuffed stained areas.
minutes. Rinse with a water-dampened cloth to remove
any remaining bleach concentration.
Rinse with a water-dampened cloth to remove cleaner CAUTION: WHEN THE USE OF STRONG CLEANING
4
SOLUTIONS IS NECESSARY, TEST AN
solution and allow thorough drying of material.
INCONSPICUOUS AREA TO ASSURE THAT
DAMAGE TO UPHOLSTERY OR PAINTED
***See current CDC Guideline for Disinfection & Sterilization in SURFACES WILL NOT OCCUR.
Healthcare Facilities for bleach alternative cleaners.

Upholstery with PreFixx® › Clorox® Healthcare VersaSure® › Diversey™ Accel®

Cleaner Disinfection Wipes INTERVention® Wipes
Protective Finish
› Clorox® Hydrogen Peroxide › Diversey™ Avert® Sporicidal
In laboratory testing, upholstery Cleaner Disinfectant Spray Disinfectant Cleaner
protected with PreFixx® finish › Clorox® Hydrogen Peroxide › ERC Performance Wipes
was treated with the following Cleaner Disinfectant Wipes
› McKesson Disposable
disinfectants with little to no › Agar™ Powerquat Germicidal Surface Wipes
discoloration or damage to the › Asepticare™ › McKesson Pro-Tech RTU
upholstery. This testing may not
› Asepticare™ TB-II Disinfectant Cleaner
reflect actual results in the field.*
› AVISTAT-D™ Ready To Use › OPTIM® 1 Wipes
Spray Disinfectant Cleaner › OPTIM® 33TB
Recommended Disinfectants
› Biotrol BirexSE ®
› Oxivir® 1 RTU
› Clorox® Broad Spectrum Quaternary
Disinfectant Cleaner › Bleach 1:5 (20% bleach)
› Oxivir® Five 16
› Clorox® Healthcare Bleach › Bleach 1:9 (10% bleach)
› Oxivir® TB
Germicidal Cleaner › Bleach-Rite® Disinfecting Spray
› OxyCide™ Daily
› Clorox® Healthcare Bleach › CaviCide™ Disinfectant Cleaner
Germicidal Wipes › CaviCide1™ › PDI Sani-Cloth® AF3
› Clorox Healthcare EZ-KILL Wipes
® ®
› CaviCide™ AF Germicidal Disposable Wipes

16
EQUIPMENT CARE

› PDI Sani-Cloth® HB › Virox PREempt™ RTU › Mr. Clean / Flash

› PDI Sani-Cloth® Plus › Virex® II 256 Clean and Shine
(Procter and Gamble)
› PDI Sani-Cloth® Prime › Virex® Plus One-Step
Germicidal Disposable Wipe Disinfectant Cleaner & Deodorant › Eco Touch All Purpose
Premium Care
› PDI Super Sani-Cloth® › Wayne® Concept 256N
› PDI Super Sani-Cloth® Bleach › Wex-Cide 128 For more difficult stains, contact
Germicidal Disposable Wipes UMF Medical Customer Service.
› Precise QTB Spray
Care & Cleaning *All disinfectants and cleaning agents
› PROCHEM® Oxy Plus Use one of the following cleaners contain chemicals that degrade coated
› Purell® Healthcare Surface Disinfectant with a soft cloth or damp sponge. fabric upholstery to some extent. To promote
› Purell® Multi-Surface Disinfectant Rinse area with fresh water then a long product life, it is recommended that
dry with a clean, lint-free cloth. the PreFixx cleaning and maintenance
› Sani Professional® Cleaning +
Degreasing Multi-Surface Wipes protocol be employed regularly.
Primary Recommended Cleaner
› Sani Professional® Multi-Surface **Inclusion in this document does not
› Formula 409 All-
Cleaning Wipes imply “fit for use.” Customers should first
Purpose spray cleaner
determine if products are appropriate for
› Sani Professional® No-Rinse › Fantastik spray cleaner use on their surfaces.
Sanitizing Multi-Surface Wipes
› SaniZide® Plus Secondary
Recommended Cleaners
› STERI-7 XTRA CONCENTRATE
(recommended dilution ratio 1:10) › Lysol Clean and Fresh
Multi-Surface Cleaner
› STERI-7 XTRA WIPES
(Reckitt Benckiser)
› Vert-2-Go ED
› Lestoil Heavy Duty
› Virox AHP 5 Cleaner (Clorox)

QUESTIONS, COMMENTS OR SERVICE REQUESTS

Contact:
UMF Medical Customer Service Toll Free: 1(800) 638-5322
1316 Eisenhower Blvd Email: [email protected]
Johnstown, PA 15904 Fax: 1(814) 266-1870

* For service requests, please have model % serial number available.

DISPOSAL INFORMATION

1 When 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.
2 Metal, plastic, and other components of table can be disassembled
and recycled if desired.

17
WARRANTY INFORMATION

Warranty Program accident, freight damage, tampering or failure to seek

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

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Ph: 814.266.8726 | Fax: 814.266.1870
1316 Eisenhower Blvd. Johnstown, PA 15904 UMFmedical.com
[email protected]