BS EN 60601-3-1:1997
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
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Medical electrical equipment. Particular requirements for performance Specification for transcutaneous oxygen and carbon dioxide partial pressure monitoring equipment
Hardcopy , PDF
15-06-2000
English
15-04-1997
INTRODUCTION
1 Scope and object
2 Normative references
3 Definitions
4 Test conditions
5 Accompanying documents
6 Accuracy
7 Response time
8 Recorder
9 Warning signals
10 Internal electrical power source
11 Transducers and cables
Figures
1 Suggested test fixture for transducer test, if the
manufacturer does not recommend another test
chamber
2 Test cycle for linearity test - Example of typical
results
Annex A (informative) Guidance and rationale
Annex ZA (normative) Normative references to international
publications with their corresponding European
publications
Defines essential requirements for performance of transcutaneous oxygen and carbon dioxide partial pressure monitoring equipment. Applicable to transcutaneous monitors for foetal monitoring during birth. ALSO NUMBERED AS BS EN 5724 SECTION 3.101 1997
Committee |
CH/62/4
|
DevelopmentNote |
DRAFT FOR COMMENT 93/503826 DC
|
DocumentType |
Standard
|
Pages |
18
|
PublisherName |
British Standards Institution
|
Status |
Superseded
|
SupersededBy | |
Supersedes |
Standards | Relationship |
NF EN 60601-3-1 : 2002 | Identical |
I.S. EN 60601-3-1:1998 | Identical |
SN EN 60601-3-1 : 1996 | Identical |
EN 60601-3-1:1996 | Identical |
BS 5724-3.101(1997) : 1997 | Identical |
UNE-EN 60601-3-1:1997 | Identical |
DIN EN 60601-3-1:1998-11 | Identical |
IEC 60601-3-1:1996 | Identical |
IEC 60601-1:2005+AMD1:2012 CSV | Medical electrical equipment - Part 1: General requirements for basic safety and essential performance |
IEC 60601-2-23:2011 | Medical electrical equipment - Part 2-23: Particular requirements for the basic safety and essential performance of transcutaneous partial pressure monitoring equipment |
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