ANSI/AAMI/IEC 60601-1-12:2016
Current
The latest, up-to-date edition.
MEDICAL ELECTRICAL EQUIPMENT - PART 1-12: GENERAL REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE - COLLATERAL STANDARD: REQUIREMENTS FOR MEDICAL ELECTRICAL EQUIPMENT AND MEDICAL ELECTRICAL SYSTEMS INTENDED FOR USE IN THE EMERGENCY MEDICAL SERVICES ENVIRONMENT
Hardcopy , PDF
English
06-10-2016
Glossary of equivalent standards
Committee representation
Background on AAMI adoption of IEC 60601-1-12:2014
Foreword
Introduction
1 Scope, object and related standards
2 Normative references
3 Terms and definitions
4 General requirements
5 Classification of ME EQUIPMENT and ME SYSTEMS
6 ME EQUIPMENT identification, marking and documents
7 Protection against electrical HAZARDS from ME EQUIPMENT
8 Protection against excessive temperatures and other
HAZARDS
9 Accuracy of controls and instruments and protection
against hazardous outputs
10 Construction of ME EQUIPMENT
11 Additional requirements for electromagnetic compatibility
of ME EQUIPMENT and ME SYSTEMS
Annex A (informative) - General guidance and rationale
Annex B (informative) - Guide to marking and labelling
requirements for ME EQUIPMENT and ME SYSTEMS
Annex C (informative) - Symbols on marking
Bibliography
Index of defined terms used in this collateral standard
Pertains to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL ELECTRICAL EQUIPMENT and MEDICAL ELECTRICAL SYSTEMS, hereafter referred to as ME EQUIPMENT and ME SYSTEMS, which are intended, as indicated in the instructions for use by their MANUFACTURER, for use in the EMS ENVIRONMENT.
| DevelopmentNote |
New child AMD 1 2021 is added.
|
| DocumentType |
Standard
|
| ISBN |
1-57020-624-4
|
| Pages |
64
|
| ProductNote |
New child AMD 1 2021 is added.
|
| PublisherName |
Association for the Advancement of Medical Instrumentation
|
| Status |
Current
|
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