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10 Technical Specifications

Breas HA 01 Humidifier User Manual

Doc. 004221 En T-2

5.2 Compliance of Standards   

S

TANDARD

S

PECIFICATIONS

IEC 60601-1 (1988)
A1 (1991)
A2 (1995)

Medical electrical equipment - Part 1: General
requirements for safety.

IEC 60601-1-1 (2000)

Medical electrical equipment - Part 1-1: Gen-
eral requirements for safety - Collateral stand-
ard: Safety requirements for medical electrical
systems.

IEC 60601-1-2 (2001)

Medical electrical equipment - Part 1-2: Gen-
eral requirements for safety - Collateral stand-
ard: Electromagnetic compatibility -
Requirements and tests.

IEC 60601-1-4 (2000)

Medical electrical equipment - Part 1-4: Gen-
eral requirements for safety - Collateral Stand-
ard: Programmable electrical medical systems.

IEC 60601-1-6 (2004)

Medical electrical equipment - Part 1-6: Gen-
eral requirements for safety - Collateral stand-
ard: Usability.

ISO 8185 (1997)
C1(2001)

Humidifiers for medical use - General require-
ments for humidification systems.

C

LASSIFICATIONS

S

PECIFICATIONS

Class IIa

Classification according to the European
Medical Device Directive 93/42/EEC.

Class II

FDA classification

Class II (IEC 60601-1) Class
II, Type BF

Electrical equipment with dual isolation and
body floating (isolated) applied part according
to IEC 60601-1.

IPX1

Degree of protection provided by enclosure.

The humidifier and its packaging do not contain any natural rubber latex.

Summary of Contents for HA 01

Page 1: ...ded to humidify the patient air User Manual for Breas HA 01 Humidifier Read this manual thoroughly so that you completely understand how the humidifier is operated and maintained before taking it into...

Page 2: ...highlight specific information The meaning of each icon is explained in the table below For complete instructions how to operate the humdifier refer to the Breas breathing therapy equipment manual IC...

Page 3: ...ated humidifier may require the installation of a water trap in the circuit The water trap prevents any condensated water in the patient circuit from run ning into the patient airways and causing pers...

Page 4: ...below 10 RH room humidity and above 95 RH atmosphere pressure below 700 mbar and above 1060 mbar The humidifier any accessories and all replaced parts must be disposed of in accordance with the local...

Page 5: ...quipment Designation and Safety Label NO COMPONENT FUNCTION 1 Humidifier lid Sealing the humidifier 2 Internal pipe To prevent water spillage into the Breas breathing therapy equipment 3 Swivel Patien...

Page 6: ...it may be returned to Breas Medical AB for scrap ping and should not be discarded with the household waste Never add or pour out water from the humidifier when attached to the Breas breathing therapy...

Page 7: ...difier can be disinfected with Virkon or Lysetol 4 1 Disposal The humidifier any accessories and all replaced parts must be disposed of and recycled in accordance with the local environmental regulati...

Page 8: ...NTAL CONDITIONS SPECIFICATION Operating temperature range 5 to 40 C 41 to 104 F Storage and transport tem perature 20 to 60 C 4 to 140 F Ambient pressure range 700 to 1060 mbar Humidity 10 to 95 non c...

Page 9: ...output of the humidifier at the patient end of the tube The warm up time for the delivered gas temperature to reach the set tempera ture from a starting temperature of 23 2 C is less than 60 minutes w...

Page 10: ...1 4 2000 Medical electrical equipment Part 1 4 Gen eral requirements for safety Collateral Stand ard Programmable electrical medical systems IEC 60601 1 6 2004 Medical electrical equipment Part 1 6 Ge...

Page 11: ...11 Notes Breas HA 01 Humidifier User Manual Doc 004221 En T 2 6 Notes...

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