IEC 80601-2-58:2014+AMD1:2016 CSV
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.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 2-58: Particular requirementsfor the basic safety and essential performance of lens removal devices and vitrectomy devices for ophthalmic surgery
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06-03-2024
English - French
20-10-2016
IEC 80601-2-58:2014+A1:2016 applies to the basic safety and essential performance of lens removal devices and vitrectomy devices for ophthalmic surgery and associated accessories that can be connected to this medical electrical equipment, hereafter referred to as ME equipment. Hazards inherent in the intended physiological function of ME equipment or ME systems within the scope of this standard are not covered by specific requirements in this standard except in 7.2.13 and 8.4.1 of the general standard. This second edition includes changes in order to take into account the commentssubmitted during the approval of the first edition as a European Medical Device Directive, as well as the comments from other National Committees during the finalization of the first edition of this standard. This consolidated version consists of the second edition (2014) and its amendment 1 (2016). Therefore, no need to order amendment in addition to this publication.
DevelopmentNote |
Stability Date: 2024. (10/2016)
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DocumentType |
Standard
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Pages |
133
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PublisherName |
International Electrotechnical Committee
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Status |
Superseded
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SupersededBy | |
Supersedes |
Standards | Relationship |
PN EN 80601-2-58 : 2015 | Identical |
ANSI/AAMI/IEC 80601-2-58:2014 | Identical |
DIN EN 80601-2-58 : 2015 | Identical |
ANSI/AAMI/IEC 80601-2-58:2014/A1:2016 | Identical |
NEN EN IEC 80601-2-58 : 2015 | Identical |
EN 80601-2-58:2015 | Identical |
NBN EN 80601-2-58 : 2015 | Identical |
BS EN 80601-2-58:2015 | Identical |
IS/IEC 80601 : Part 2 : Sec 58 : 2016 | Identical |
VDE 0750-2-58 : 2015 | Identical |
UNE-EN 80601-2-58:2009 | Identical |
IEC 60950-1:2005+AMD1:2009+AMD2:2013 CSV | Information technology equipment - Safety - Part 1: General requirements |
ISO 11607-2:2006 | Packaging for terminally sterilized medical devices Part 2: Validation requirements for forming, sealing and assembly processes |
ISO 15752:2010 | Ophthalmic instruments Endoilluminators Fundamental requirements and test methods for optical radiation safety |
IEC 60825-1:2014 | Safety of laser products - Part 1: Equipment classification and requirements |
IEC 61847:1998 | Ultrasonics - Surgical systems - Measurement and declaration of the basic output characteristics |
IEC 60601-2-22:2007+AMD1:2012 CSV | Medical electrical equipment - Part 2-22: Particular requirements for basic safety and essential performance of surgical, cosmetic, therapeutic and diagnostic laser equipment |
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/TR 16142:2006 | Medical devices Guidance on the selection of standards in support of recognized essential principles of safety and performance of medical devices |
IEC TR 60878:2015 | Graphical symbols for electrical equipment in medical practice |
CISPR 11:2015 RLV | Industrial, scientific and medical equipment - Radio-frequency disturbance characteristics - Limits and methods of measurement |
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 |
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