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5

Test specifications for Enclosure Port Immunity to RF wireless communications equipment

Test  

frequency

Band 

a)

Service 

a)

Modulation 

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

9

745

780

810

800 – 960

GSM 800/900, TETRA 
800, iDEN 820, CDMA 
850, LTE  Band 5

Pulse modulation 

b)

18 Hz

2

0,3

28

870

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

9

5 500

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.

Summary of Contents for FUSIONONE 3001

Page 1: ...TURE MAXIMUM PATIENT WEIGHT 500 LBS 226 KG UMFmedical com Ph 814 266 8726 Fax 814 266 1870 1316 Eisenhower Blvd Johnstown PA 15904 customerservice umfmedical com OWNER S MANUAL FUSIONONE POWER EXAM CHAIR 3001 3002 3003 3 2518 Rev A ...

Page 2: ...CSA CAN CSA C22 2 NO 60601 1 14 IEC 60601 1 Edition 3 1 2012 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 CLASSIFICATIONS APPLIED PARTS IMPORTA...

Page 3: ...h 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 ENVIRON...

Page 4: ...ne 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 PERFOR...

Page 5: ...ve 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 ...

Page 6: ...pply 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 ...

Page 7: ...A SEAT BACKREST IS NOT DESIGNED TO SUPPORT PATIENT S FULL WEIGHT WARNING Hand Foot Control Table Operation FEATURES AND OPERATION Hand Control Foot Control Table High Low Function Operation 1 Press the up button to raise the table 2 Press the down button to lower the table DO NOT PLACE FOOT REST ON BASE DURING OPERATION WARNING Optional accessory 581 ...

Page 8: ... drawer for cleaning purposes 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 DO NOT USE DRAWER OR DRIP PAN AS A SEAT OR STEP WARNING DO NOT USE THE LEG REST AS A SEAT OR STEP WARNING FEATURES AND OPERATION Products placed in warming drawer should be checked for proper temperature befo...

Page 9: ...Release stirrup to lock into position 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 DO NOT SUPPORT THE PATIENT S ENTIRE WEIGHT WITH THE STIRRUPS ENSURE STIRRUPS ARE PROPERLY LOCKED ...

Page 10: ...e 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 ...

Page 11: ... 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 COMMON OPTIONS AND ACCESSORIES 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 WARNING ...

Page 12: ...ULD NOT BE USED FOR ANY OTHER ITEMS 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 WARNING GROUND RELIABILITY CAN ONLY BE ACHIEVED WHEN POWER SUPPLY IS CONNECTED TO AN EQUIVALENT RECEPTACL...

Page 13: ...ES 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 ...

Page 14: ...ABLE 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 ...

Page 15: ... 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 ...

Page 16: ...S NECESSARY TEST AN INCONSPICUOUS AREA TO ASSURE THAT DAMAGE TO UPHOLSTERY OR PAINTED SURFACES WILL NOT OCCUR CAUTION Proper Sterilization Instructions Upholstery with PreFixx Protective 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 AVIS...

Page 17: ...fessional 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 Care Cleaning Use one of the following cleaners with a soft cloth or damp sponge Rinse area with fresh water then dry wit...

Page 18: ...ns 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...

Page 19: ...19 This page intentionally left blank ...

Page 20: ...UMFmedical com Ph 814 266 8726 Fax 814 266 1870 1316 Eisenhower Blvd Johnstown PA 15904 customerservice umfmedical com ...

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