GSO ISO 18113-4:2016

ISO 18113-4:2009
Gulf Standard   Historical · Approved on 22 December 2016

In vitro diagnostic medical devices -- Information supplied by the manufacturer (labelling) -- Part 4: In vitro diagnostic reagents for self-testing

GSO ISO 18113-4:2016 Files

English 10 Pages
Historical Reference Language
30.05 OMR

GSO ISO 18113-4:2016 Scope

This part of ISO 18113 specifies requirements for information supplied by the manufacturer of IVD reagents for self-testing. This part of ISO 18113 also applies to information supplied by the manufacturer with calibrators and control materials intended for use with IVD medical devices for self-testing. This part of ISO 18113 can also be applied to accessories. This part of ISO 18113 applies to the labels for outer and immediate containers and to the instructions for use. This part of ISO 18113 does not apply to: a) IVD instruments or equipment, b) IVD reagents for professional use.

Best Sellers From Health Sector

GSO 2017:2023
 
Gulf Standard
Personal Care and Baby Wet Wipes
GSO 2241:2023
 
Gulf Standard
Cosmetic Products - Body Cleaners
GSO 2063:2023
 
Gulf Standard
Cosmetic Products - Hair Conditioner (Balsam)
GSO 1223:2023
 
Gulf Standard
Cosmetic Products-Deodorants

Recently Published from Health Sector

GSO ISO 10993-10:2024
ISO 10993-10:2021 
Gulf Standard
Biological evaluation of medical devices — Part 10: Tests for skin sensitization
GSO ISO 21649:2024
ISO 21649:2023 
Gulf Standard
Needle-free injection systems for medical use — Requirements and test methods
GSO ISO 15854:2024
ISO 15854:2023 
Gulf Standard
Dentistry — Casting and baseplate waxes
GSO IEC TR 60878:2024
IEC TR 60878:2022 
Gulf Standard
Graphical symbols for electrical equipment in medical practice