Abstract
IEC 80601-2-58:2014 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 comments submitted 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.
General information
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Status: PublishedPublication date: 2014-09Stage: International Standard to be revised [90.92]
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Edition: 2Number of pages: 56
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Technical Committee :ISO/TC 172/SC 7ICS :11.040.70
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Life cycle
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Previously
WithdrawnIEC 80601-2-58:2008
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Now
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00
Preliminary
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10
Proposal
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20
Preparatory
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30
Committee
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40
Enquiry
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50
Approval
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60
Publication
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90
Review
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95
Withdrawal
Corrigenda / Amendments
PublishedIEC 80601-2-58:2014/Amd 1:2016
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00
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Will be replaced by
Under developmentIEC/FDIS 80601-2-58
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