EN 80601-2-58:2015/A1:2019
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
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
01-03-2024
23-08-2019
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.
Committee |
CLC/TC 62
|
DocumentType |
Amendment
|
ProductNote |
THIS STANDARD ALSO REFERS - EN ISO 11607-1:2009/A1:2014,EN ISO 11607-2:2006/A1:2014
|
PublisherName |
European Committee for Standards - Electrical
|
Status |
Superseded
|
Standards | Relationship |
DIN EN 80601-2-58 : 2020 | Identical |
I.S. EN 80601-2-58:2015/A1:2019 | Identical |
OVE EN 80601-2-58:2020 07 01 | Identical |
VDE 0750-2-58:2020-06 | Identical |
BS EN 80601-2-58:2015+A1:2019 | Identical |
BS EN IEC 61784-3-2:2021 | Identical |
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