NF EN 80601-2-58:2015
Current
Current
The latest, up-to-date edition.
MEDICAL ELECTRICAL EQUIPMENT - PART 2-58: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF LENS REMOVAL DEVICES AND VITRECTOMY DEVICES FOR OPHTHALMIC SURGERY
Amended by
Available format(s)
Hardcopy
Language(s)
French, English - French
Published date
01-09-2015
Publisher
Important note : Users cannot be edited or removed once added to your Multi user PDF.| Committee |
SC 62D
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| DevelopmentNote |
Indice de classement: C74-395. PR NF EN 80601-2-58 January 2008. (01/2008) PR NF EN 80601-2-58 June 2013. (07/2013) 2009 version along with its amendment is still active. (09/2015)
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| DocumentType |
Standard
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| Pages |
32
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| ProductNote |
New child AMD 1 2019 is added
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| PublisherName |
Association Francaise de Normalisation
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| Status |
Current
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| Standards | Relationship |
| EN 80601-2-58:2015 | Identical |
| IEC 80601-2-58:2014 | Identical |
| NF EN 61847 : 2006 | ULTRASONICS - SURGICAL SYSTEMS - MEASUREMENT AND DECLARATION OF THE BASIC OUTPUT CHARACTERISTICS |
| ISO 11607-2:2006 | Packaging for terminally sterilized medical devices Part 2: Validation requirements for forming, sealing and assembly processes |
| IEC 61847:1998 | Ultrasonics - Surgical systems - Measurement and declaration of the basic output characteristics |
| NF EN 60601-1-2 : 2016 | MEDICAL ELECTRICAL EQUIPMENT - PART 1-2: GENERAL REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE - COLLATERAL STANDARD: ELECTROMAGNETIC DISTURBANCES - REQUIREMENTS AND TESTS |
| IEC 60601-1-2:2014 | Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests |
| IEC 60601-2-2:2017 | Medical electrical equipment - Part 2-2: Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories |
| ISO 11607-1:2006 | Packaging for terminally sterilized medical devices Part 1: Requirements for materials, sterile barrier systems and packaging systems |
| ISO 17664:2017 | Processing of health care products Information to be provided by the medical device manufacturer for the processing of medical devices |
| NF EN 60601-2-2 : 2009 AMD 11 2012 | MEDICAL ELECTRICAL EQUIPMENT - PART 2-2: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF HIGH FREQUENCY SURGICAL EQUIPMENT AND HIGH FREQUENCY SURGICAL ACCESSORIES |
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