GSO ISO 6717:2024

ISO 6717:2021
Gulf Standard   Current Edition · Approved on 25 April 2024

In vitro diagnostic medical devices — Single-use containers for the collection of specimens from humans other than blood

GSO ISO 6717:2024 Files

English 14 Pages
Current Edition Reference Language
46.91 OMR

GSO ISO 6717:2024 Scope

This document specifies requirements and test methods for specialized single-use evacuated and non-evacuated containers, intended by their manufacturers, for the primary containment and preservation of specimens, other than blood specimens, derived from the human body, for the purposes of in vitro diagnostic examination. It is not intended to cover specimen containers for forensic investigations.

Examples of such specimens include, but are not limited to, cerebral spinal fluid (CSF), faeces, infected bodily fluids, saliva, ejaculate, sputum, urine, tissue samples.

Specimens and types of devices specifically excluded are specialized containers for cryo-preservation, samples for nucleic acid testing and swabs.

NOTE       Requirements and test methods for evacuated and non-evacuated single-use human venous blood specimen collection containers are specified in ISO 6710.

This document does not specify requirements for auxiliary devices used in conjunction with specimen containers.

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/TS 24665:2025
ISO/TS 24665:2023 
Gulf Standard
Playground and recreational areas — Framework for the competence of playground inspectors and playground maintenance technicians
GSO ISO 8536-13:2025
ISO 8536-13:2024 
Gulf Standard
Infusion equipment for medical use — Part 13: Graduated flow regulators for single use with fluid contact
GSO ISO 18562-3:2025
ISO 18562-3:2024 
Gulf Standard
Biocompatibility evaluation of breathing gas pathways in healthcare applications — Part 3: Tests for emissions of volatile organic substances
GSO IEC TS 60601-4-6:2025
IEC TS 60601-4-6:2024 
Gulf Standard
Medical electrical equipment - Part 4-6: Guidance and interpretation - Voluntary guidance to help achieve basic safety and essential performance with regard to the possible effects of electromagnetic disturbances