ISO 29061-5:2026

International Standard   Current Edition · Approved on 06 February 2026

Road vehicles — Methods and criteria for usability evaluation of child restraint systems and their interface with vehicle anchorage systems — Part 5: Installation and securing of child in a booster system

ISO 29061-5:2026 Files

English 21 Pages
Current Edition
BHD 61.53

ISO 29061-5:2026 Scope

This document provides criteria for judgement of usability of booster seat child restraint systems (CRSs) when installing them and securing a child.

This document provides criteria for judgement of:

  • ease of availability of instructions;
  • clarity of instruction manual and labelling; and
  • ease of use of design related features of the CRS related to the installation in a vehicle.

The procedure can also be used for evaluation of vehicle integrated booster systems.

NOTE 1        CRS includes enhanced child restraint systems (ECRS) according to UN Regulation No. 129.

NOTE 2        Although ISOFIX is defined in the original “ISOFIX” standard (ISO 13216-1) to be a rigid system, the term “ISOFIX” in this document is extended to include flexible CRS attachments (e.g. LATCH in USA, UAS in Canada).

Best Sellers

GSO 150-2:2013
 
Gulf Standard
Expiration dates for food products - Part 2 : Voluntary expiration dates
BH GSO 150-2:2015
GSO 150-2:2013 
Bahraini Standard
Expiration dates for food products - Part 2 : Voluntary expiration dates
GSO 9:2022
 
Gulf Technical Regulation
Labeling of prepackaged food stuffs
BH GSO 9:2023
GSO 9:2022 
Bahraini Technical Regulation
Labeling of prepackaged food stuffs

Recently Published

ISO 18615-1:2026
 
International Standard
Traditional Chinese medicine — Electric radial pulse tonometric devices — Part 1: General requirements
ISO 21388-1:2026
 
International Standard
Acoustics — Hearing aid fitting management (HAFM) — Part 1: General process
ISO 20915:2026
 
International Standard
Life cycle inventory calculation methodology for steel products
ISO 11607-3:2026
 
International Standard
Packaging for terminally sterilized medical devices — Part 3: Requirements for process development for forming, sealing and assembly