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CEI EN 60601-2-13 : 2007

Withdrawn
Withdrawn

A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.

MEDICAL ELECTRICAL EQUIPMENT - PART 2: PARTICULAR REQUIREMENTS FOR THE SAFETY AND ESSENTIAL PERFORMANCE OF ANAESTHETIC SYSTEMS
Available format(s)

Hardcopy , PDF

Withdrawn date

07-01-2020

Language(s)

English - Italian

Published date

01-01-2007

INTRODUCTION
SECTION ONE - GENERAL
SECTION TWO - ENVIRONMENTAL
              CONDITIONS
SECTION THREE - PROTECTION
                AGAINST ELECTRIC
                SHOCK HAZARDS
SECTION FOUR - PROTECTION AGAINST
               MECHANICAL HAZARDS
SECTION FIVE - PROTECTION AGAINST
               HAZARDS FROM UNWANTED
               OR EXCESSIVE RADIATION
SECTION SIX - PROTECTION AGAINST
              HAZARDS OF IGNITION
              OF FLAMMABLE ANAESTHETIC
              MIXTURES
SECTION SEVEN - PROTECTION AGAINST
                EXCESSIVE TEMPERATURES
                AND OTHER SAFETY HAZARDS
SECTION EIGHT - ACCURACY OF OPERATING
                DATA AND PROTECTION
                AGAINST HAZARDOUS OUTPUT
SECTION NINE - ABNORMAL OPERATION
               AND FAULT CONDITIONS
               ENVIRONMENTAL TESTS
SECTION TEN - CONSTRUCTIONAL REQUIREMENTS
SECTION 101 - ADDITIONAL CLAUSES
              SPECIFIC TO ANAESTHETIC
              GAS DELIVERY SYSTEMS
Annex AA (informative) - Guidance and
         rationale for particular
         clauses and subclauses in
         this particular standard
Annex BB (informative) - MONITORING
         DEVICES, ALARM SYSTEM(S) and
         PROTECTION DEVICES
Annex CC (informative) - Separate
         devices of an ANAESTHETIC
         SYSTEM
Annex DD (normative) - Test for
         flammability of anaesthetic
         agent
Annex EE (informative) - Clauses of
         this International Standard
         addressing the essential
         requirements or other provisions
         of EU directives
Bibliography
Index of defined terms
Annex ZA (normative) - Normative
         references to international
         publications with their
         corresponding European
         publications
Annex ZZ (informative) - Coverage
         of Essential Requirements
         of EC Directives

Specifies safety and essential performance requirements for an ANAESTHETIC SYSTEM as well as individual devices designed for use in an ANAESTHETIC SYSTEM.

Committee
CT 62
DevelopmentNote
Classificazione CEI 62-142. (12/2006)
DocumentType
Standard
Pages
98
PublisherName
Comitato Elettrotecnico Italiano
Status
Withdrawn

Standards Relationship
IEC 60601-2-13:2003+AMD1:2006 CSV Identical
EN 60601-2-13 : 2006 AMD 1 2007 Identical

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ISO 9703-2:1994 Anaesthesia and respiratory care alarm signals — Part 2: Auditory alarm signals
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ISO 15223:2000 Medical devices Symbols to be used with medical device labels, labelling and information to be supplied
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