Log inSign up
LANGUAGE en
Menu
STOREHelp centerContactsDelivery chargesABOUT US News
SEARCH
0
Total price
0 EUR
PRICES include / exclude VAT
>BSI Standards >11 HEALTH CARE TECHNOLOGY>11.040 Medical equipment>11.040.50 Radiographic equipment>BS EN IEC 60601-2-57:2026+A11:2026 Medical electrical equipment Particular requirements for the basic safety and essential performance of non-laser light source equipment intended for therapeutic, diagnostic, monitoring, cosmetic and aesthetic use
immediate downloadReleased: 2026-02-23
BS EN IEC 60601-2-57:2026+A11:2026 Medical electrical equipment Particular requirements for the basic safety and essential performance of non-laser light source equipment intended for therapeutic, diagnostic, monitoring, cosmetic and aesthetic use

BS EN IEC 60601-2-57:2026+A11:2026

Medical electrical equipment Particular requirements for the basic safety and essential performance of non-laser light source equipment intended for therapeutic, diagnostic, monitoring, cosmetic and aesthetic use

Format
Availability
Price and currency
English Secure PDF
Immediate download
Printable - You are authorized to print 1 copy
304.64 EUR
English Hardcopy
In stock
304.64 EUR
Standard number:BS EN IEC 60601-2-57:2026+A11:2026
Pages:40
Released:2026-02-23
ISBN:978 0 539 37424 7
Status:Standard
DESCRIPTION

BS EN IEC 60601-2-57:2026+A11:2026


This standard BS EN IEC 60601-2-57:2026+A11:2026 Medical electrical equipment is classified in these ICS categories:
  • 29.240.01 Power transmission and distribution networks in general
  • 29.080.01 Electrical insulation in general
  • 17.220.20 Measurement of electrical and magnetic quantities
  • 11.040.60 Therapy equipment
  • 11.040.50 Radiographic equipment
The amendment to EN IEC 60601-2-57 contains the Annexes ZA (Normative references to international publications with their corresponding European publications) and ZZ (Relationship between this European standard and the General Safety and Performance Requirements of Regulation (EU) 2017/745 aimed to be covered). These two Annexes are necessary for the harmonization of the standard to the Regulation (EU) 2017/745.
Print