Перейти к содержимому
Low prices. Originals and translations — save time and budget.

IEC 80601-2-89:2025 PDF

Medical electrical equipment — Part 2-89: Particular requirements for the basic safety and essential performance of medical beds for children

First page of standard IEC 80601-2-89:2025Open preview (PDF)Medical electrical equipment — Part 2-89: Particular requirements for the basic safety and essential performance of medical beds for children
Title (English):
IEC 80601-2-89:2025

Medical electrical equipment — Part 2-89: Particular requirements for the basic safety and essential performance of medical beds for children

Document status:
Active
Format:
Electronic (PDF)
Number of pages:
214
Publication date:
December 9, 2025
Edition:
IEC IS 80601 edition 1 version 1
ICS:
11.140
Description (English):

This document applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL BEDS, hereafter referred to as MEDICAL BEDS as defined in 201.3.219, intended for CHILDREN as defined in 201.3.207, and ADULTS with atypical anatomy (ADULTS ranging outside the definition for ADULTS in 201.3.201). This document applies to both electrical and non-electrical(manual) MEDICAL BEDS with or without adjustable functions. This document applies to MEDICAL BEDS with an INTERNAL LENGTH of up to 180 cm suitable to a body length of 155 cm. If a MANUFACTURER wishes to make a bed that can be used by both a CHILD and an ADULT, e.g. INTERNAL LENGTH of 180 cm or more, then IEC 80601-2-52 and this document apply. This document does not apply to: • ADULT only beds covered by IEC 80601-2-52; • SPECIALITY MATTRESS covered by the ISO 20342 series; • incubators covered by IEC 60601-2-19; • devices for which the INTENDED USE is mainly for examination or transportation under medical supervision (e.g. stretcher, examination table). If a clause or subclause is specifically intended to be applicable to a MEDICAL BED 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 MEDICAL BEDS and to ME SYSTEMS, as relevant. HAZARDS inherent in the intended physiological function of MEDICAL BEDS or ME SYSTEMS within the scope of this document are not covered by specific requirements in this document except in IEC 60601-1:2005, IEC 60601-1:2005/AMD1:2012 and IEC 60601-1:2005/AMD2:2020, 7.2.13 and 8.4.1.

Technical details

Technical committee
ISO/TC 173 - Assistive products
SKU
IEC 80601-2-89:2025

This site uses cookies and visit counters for operation and statistics. Privacy policy