OS GSO ISO 18113-1:2024

ISO 18113-1:2022
Omani Standard   Current Edition · Approved on 14 October 2024

In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions, and general requirements

OS GSO ISO 18113-1:2024 Files

OS GSO ISO 18113-1:2024 Scope

This document defines concepts, establishes general principles, and specifies essential requirements for information supplied by the manufacturer of IVD medical devices.

This document does not address language requirements since that is the domain of national laws and regulations.

This document does not apply to:

a) IVD medical devices for performance evaluation (e.g. for investigational use only);

b) shipping documents;

c) material safety data sheets / Safety Data Sheets;

d) marketing information (consistent with applicable legal requirements).

.

Best Sellers From Health Sector

OS GSO 2017:2023
GSO 2017:2023 
Omani Standard
Personal Care and Baby Wet Wipes
GSO 2017:2023
 
Gulf Standard
Personal Care and Baby Wet Wipes
OS GSO 2241:2023
GSO 2241:2023 
Omani Standard
Cosmetic Products - Body Cleaners
GSO 2241:2023
 
Gulf Standard
Cosmetic Products - Body Cleaners

Recently Published from Health Sector

GSO ISO 22525:2025
ISO 22525:2020 
Gulf Standard
Tourism and related services — Medical tourism — Service requirements
GSO EN 16120:2012+A2:2025
EN 16120:2012+A2:2016 
Gulf Standard
Child use and care articles - Chair mounted seat
GSO ASTM F1235:2025
ASTM F1235:18 
Gulf Standard
Standard Consumer Safety Specification for Portable Hook-On Chairs
GSO ISO 24805:2025
ISO 24805:2022 
Gulf Standard
Recreational diving services — Requirements for rebreather diver training — Decompression diving to 45 m