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BS EN ISO 6717:2021

Current

Current

The latest, up-to-date edition.

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

Available format(s)

Hardcopy , PDF

Language(s)

English

Published date

09-08-2021

This document specifies requirements and test methods for specialized single-use evacuated and nonevacuated 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.

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 ISO6710 .This document does not specify requirements for auxiliary devices used in conjunction with specimen containers.

Committee
CH/212
DocumentType
Standard
ISBN
9780539147179
Pages
22
ProductNote
This standard also refers to BS EN ISO 15223-1
PublisherName
British Standards Institution
Status
Current
Supersedes

Standards Relationship
ISO 6717:2021 Identical
EN ISO 6717:2021 Identical

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