AS/NZS 3200.2.23:2001
Superseded
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Medical electrical equipment Particular requirements for safety - Transcutaneous partial pressure monitoring equipment
Hardcopy , PDF 1 User , PDF 3 Users , PDF 5 Users , PDF 9 Users
English
11-12-2001
07-29-2024
Specifies the particular requirements for the safety, including essential performances, of transcutaneaous partial pressure monitoring equipment, and applies to equipment used with adults, children and neonates, including their use in foetal monitoring during birth. It does not apply to haemoglobin saturation oximeters or to devices applied to surfaces of the body other than the skin. This Standartd is to be read in conjunction with AS/NZS 3200.1.0:1998. It is identical with, and reproduced from, IEC 60601-2-23:1999.
| Committee |
HE-003
|
| DocumentType |
Standard
|
| ISBN |
0 7337 4039 1
|
| Pages |
30
|
| ProductNote |
Pending Revision indicates that as a result of the Aged Standards review process, the document needs updating. If no project proposal, meeting the quality criteria, is received within the 12 month timeframe, the document shall be withdrawn.
|
| PublisherName |
Standards Australia
|
| Status |
Superseded
|
| SupersededBy | |
| Supersedes |
| Standards | Relationship |
| IEC 60601-2-23:1999 | Identical |
First published as Joint Standard AS/NZS 3200.2.23:1994.
Second edition 2001.
A newer version of this standard is available.
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