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PN MN234 G | User Manual    13 - ENG

Liberator

Table 4

Guidance and Manufacturer’s Declaration—Immunity ME Equipment and ME Systems

Guidance and Manufacturer’s Declaration—Immunity
The Liberator is intended for use in the electromagnetic environment specified below. The customer or 

user of the Liberator should ensure that it is used in such an environment.

Immunity Test

IEC 60601 Test Level

Compliance Level

Electromagnetic Environment—Guidance

Conducted RF IEC 

61000-4-6

Radiated RF IEC 

61000-4-3

3 Vrms

6 Vrms (In ISM Bands)

150 kHz to 80 MHz

80 MHz to 2.7 GHz

Not applicable
Battery powered 

device, No SIP/SOP

10 V/m
80 MHz—2,7 GHz
80 % AM at 1 kHz

Portable and mobile RF communications 

equipment should be used no closer to any 

part of the Liberator, including cables, than the 

recommended separation distance calculated 

from the equation applicable to the frequency 

of the transmitter.

Recommended separation distance

d = 1,2 

P

d = 1,2 

P

d = 2,3 

P

where P is the maximum output power rating 

of the transmitter in watts (W) according to the 

transmitter manufacturer and d is the recom-

mended separation distance in meters (m).

Field strengths from fixed RF transmitters, as 

determined by an electromagnetic site survey

a

should be less than the compliance level in 

each frequency range

b

.

  

 

Interference may occur in the vicinity of equip-

ment marked with the following symbol:

Test frequency 

(MHz)

Band

a)

(MHz)

Service

a)

Modulation

b)

Maximum 

power (W)

Distance 

(m)

Immunity Test 

Level (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

1720

1700–

1900

GSM 1800; CDMA 1900; 

GSM 1900; DECT; LTE 

Band 1, 3, 4, 25; UMTS

Pulse modulation

b)

217 Hz

2

0.3

28

1845
1970

2450

2400–

2570

Bluetooth, WLAN, 802.11 

b/g/n, RFID 2450, LTE 

Band 7

Pulse modulation

b)

217 Hz

2

0.3

28

5240

5100–

5800

WLAN 802.11 a/n

Pulse modulation

b)

217 Hz

0.2

0.3

9

5500
5785

NOTE: If necessary to achieve the IMMUNITY TEST LEVEL, the distance between the transmitting antenna and 
the Liberator may be reduced to 1m. The 1m 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 Liberator 20

Page 1: ...Liberator User Manual English...

Page 2: ...an Community If the product unique device identifier UDI label has the CE symbol on it the device complies with the requirements of Directive 93 42 EEC concerning medical devices The CE symbol indicat...

Page 3: ...kg 48 6 lb 22 04 kg 50 lb 22 68 kg 55 lb 24 95 kg 75 4 lb 34 19 kg Weight Filled 89 7 lb 40 69 kg 123 36 lb 56 13 kg 141 01 lb 63 98 kg 165 32 lb 74 99 kg 220 68 lb 100 1 kg Height 24 5 in 622 mm 29 5...

Page 4: ...URRED Caution Use the Liberator only as directed by your doctor Caution The unit contains liquid oxygen which is extremely cold almost 300 F 184 C Exposure to such a low temperature can cause severe f...

Page 5: ...unit which provides you with supplementary oxygen as prescribed by your physi cian This user manual contains the instructions for using the Liberator Refer to the user manual supplied with the portab...

Page 6: ...DOES NOT SEPARATE EASILY DO NOT USE FORCE THE UNITS MAY BE FROZEN TOGETHER LEAVE THE UNITS CONNECTED AND WAIT UNTIL THEY WARM UP THEN THEY WILL SEPARATE EASILY DO NOT TOUCH ANY FROSTED PARTS Caution S...

Page 7: ...Indicator lights up when the button is depressed inform your health care pro vider the next time your Liberator is filled Gen 4 Meter 5 Install the DISS extension 6 Either a Attach cannula to the DISS...

Page 8: ...g and empty as required 4 If the Portable runs low before the Liberator is fully defrosted you may refill it as needed Battery Care and Maintenance Depress button to display level If level is displaye...

Page 9: ...to time to relieve excess pressure especially soon after filling If hissing is persistent or abnormal this could indicate excess pressure being vented off or a leak in the system Contact service prov...

Page 10: ...be stored in the upright position and be well ventilated Do not allow the device to lie on its side Humidity up to 95 noncondensing Temperatures range from 40 F to 158 F 40 C to 70 C Operating temper...

Page 11: ...ovided in this manual Caution Portable and mobile radio frequency RF communications equipment can affect Medical Electrical Equipment Caution The Liberator Reservoir should not be used adjacent to or...

Page 12: ...r equipment which has been tested to specific test levels and over specific frequency ranges and been found compliant with regulations Table 3 Guidance and manufacturers declaration electromagnetic im...

Page 13: ...ned by an electromagnetic site surveya should be less than the compliance level in each frequency rangeb Interference may occur in the vicinity of equip ment marked with the following symbol Test freq...

Page 14: ...14 ENG PN MN234 G User Manual Liberator Notes...

Page 15: ...PN MN234 G User Manual 15 ENG Liberator Notes...

Page 16: ...5535 0989 Email medstar medstar com br CAIRE and CAIRE Inc are registered trademarks of CAIRE Inc Please visit our website below for a full listing of trademarks Trademarks www caireinc com corporate...

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