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DIN EN 60601-3-1:1998-11

Superseded

Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.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 - PART 3-1: ESSENTIAL PERFORMANCE REQUIREMENT FOR TRANSCUTANEOUS OXYGEN AND CARBON DIOXIDE PARTIAL PRESSURE MONITORING EQUIPMENT

Superseded date

01-11-2000

Superseded by

DIN EN 60601-2-23 : 2016

Published date

12-01-2013

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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
German Institute for Standardisation (Deutsches Institut für Normung)
Status
Superseded
SupersededBy

Standards Relationship
IEC 60601-3-1:1996 Identical
BS EN 60601-3-1:1997 Identical
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
UNE-EN 60601-3-1:1997 Identical

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