SN EN 60601-3-1 : 1996
Current
The latest, up-to-date edition.
MEDICAL ELECTRICAL EQUIPMENT - PART 3-1: ESSENTIAL PERFORMANCE REQUIREMENT FOR TRANSCUTANEOUS OXYGEN AND CARBON DIOXIDE PARTIAL PRESSURE MONITORING EQUIPMENT
12-01-2013
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
DocumentType |
Standard
|
PublisherName |
Swiss Standards
|
Status |
Current
|
Standards | Relationship |
DIN EN 60601-3-1:1998-11 | Identical |
UNE-EN 60601-3-1:1997 | Identical |
EN 60601-3-1:1996 | Identical |
BS EN 60601-3-1:1997 | Identical |
IEC 60601-3-1:1996 | Identical |
I.S. EN 60601-3-1:1998 | Identical |
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