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Homepage>BS Standards>11 HEALTH CARE TECHNOLOGY>11.040 Medical equipment>11.040.70 Ophthalmic equipment>BS EN 80601-2-58:2015+A1:2019 Medical electrical equipment Particular requirements for the basic safety and essential performance of lens removal devices and vitrectomy devices for ophthalmic surgery
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BS EN 80601-2-58:2015+A1:2019 Medical electrical equipment Particular requirements for the basic safety and essential performance of lens removal devices and vitrectomy devices for ophthalmic surgery

BS EN 80601-2-58:2015+A1:2019

Medical electrical equipment Particular requirements for the basic safety and essential performance of lens removal devices and vitrectomy devices for ophthalmic surgery

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Standard number:BS EN 80601-2-58:2015+A1:2019
Pages:40
Released:2019-09-02
ISBN:978 0 580 90617 6
Status:Standard
DESCRIPTION

BS EN 80601-2-58:2015+A1:2019


This standard BS EN 80601-2-58:2015+A1:2019 Medical electrical equipment is classified in these ICS categories:
  • 11.040.70 Ophthalmic equipment

Clause 1 of the general standard1 applies, except as follows:

201.1.1 * Scope

Replacement:

This International Standard applies to the basic safety and essential performance of lens removal devices and vitrectomy devices for ophthalmic surgery (as defined in 201.3.208 and 201.3.217) and associated accessories that can be connected to this medical electrical equipment, hereafter referred to as me equipment.

If a clause or subclause is specifically intended to be applicable to me equipment only, or to me systems only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to me equipment and to me systems, as relevant.

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.

NOTE See also 4.2 of the general standard.

201.1.2 Object

Replacement:

The object of this particular standard is to establish particular basic safety and essential performance requirements for lens removal devices and vitrectomy devices for ophthalmic surgery (as defined in 201.3.208 and 201.3.217) and associated accessories that can be connected to the me equipment and are to be tested together or individually.

201.1.3

A1_start* Collateral standardsA1_end

Addition:

This particular standard refers to those applicable collateral standards that are listed in Clause 2 of the general standard and Clause 201.2 of this particular standard.

A1_startIEC 60601‑1‑2 applies as modified in Clause 202. IEC 60601‑1‑3, IEC 60601‑1‑10, IEC 60601‑1‑11, and IEC 60601‑1‑12 do not apply.A1_end

201.1.4 Particular standards

Replacement:

In the IEC 60601 series, particular standards may modify, replace or delete requirements contained in the general standard and collateral standards as appropriate for the particular me equipment under consideration, and may add other basic safety and essential performance requirements.

A requirement of a particular standard takes priority over the general standard.

For brevity, IEC 60601‑1 is referred to in this particular standard as the “general standard”. Collateral standards are referred to by their document number.

The numbering of clauses and subclauses of this particular standard corresponds to that of the general standard with the prefix “201” (e.g. 201.1 in this standard addresses the content of Clause 1 of the general standard) or applicable collateral standard with the prefix “20x” where × is the final digit(s) of the collateral standard document number (e.g. 202.4 in this particular standard addresses the content of Clause 4 of the A1_startIEC 60601‑1‑2A1_end collateral standard, 203.4 in this particular standard addresses the content of Clause 4 of the A1_startIEC 60601‑1‑3A1_end collateral standard, etc.). The changes to the text of the general standard are specified by the use of the following words:

”Replacement” means that the clause or subclause of the general standard or applicable collateral standard is replaced completely by the text of this particular standard.

“Addition” means that the text of this particular standard is additional to the requirements of the general standard or applicable collateral standard.

“Amendment” means that the clause or subclause of the general standard or applicable collateral standard is amended as indicated by the text of this particular standard.

Subclauses, figures or tables which are additional to those of the general standard are numbered starting from 201.101. HoweverA1_start,A1_end due to the fact that definitions in the general standard are numbered 3.1 through 3.139, additional definitions in this standard are numbered beginning from 201.3.201. Additional annexes are lettered AA, BB, etc., and additional items aa), bb), etc.

Subclauses, figures or tables which are additional to those of a collateral standard are numbered starting from 20x, where “x” is the number of the collateral standard, e.g. 202 for IEC 60601‑1‑2, 203 for IEC 60601‑1‑3, etc.

The term “this standard” is used to make reference to the general standard, any applicable collateral standards and this particular standard taken together.

Where there is no corresponding clause or subclause in this particular standard, the clause or subclause of the general standard or applicable collateral standard, although possibly not relevant, applies without modification; where it is intended that any part of the general standard or applicable collateral standard, although possibly relevant, is not to be applied, a statement to that effect is given in this particular standard.