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ISO 6717:2021

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

Aug 26, 2021

General information

60.60     Aug 26, 2021

ISO

ISO/TC 76

International Standard

11.100.10  

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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.

Life cycle

NOW

PUBLISHED
ISO 6717:2021
60.60 Standard published
Aug 26, 2021

National adoptions

SRPS EN ISO 6717:2021  
ISS

In vitro diagnostic medical devices - Single-use containers for the collection of specimens from humans other than blood (ISO 6717:2021)

60.60   Standard published

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