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>UNE EN ISO 6717:2022 - In vitro diagnostic medical devices - Single-use containers for the collection of specimens from humans other than blood (ISO 6717:2021)
sklademVydáno: 2022-03-16
UNE EN ISO 6717:2022 - In vitro diagnostic medical devices - Single-use containers for the collection of specimens from humans other than blood (ISO 6717:2021)

UNE EN ISO 6717:2022

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

Productos sanitarios para diagnóstico in vitro. Recipientes de un solo uso para la recogida de muestras primarias de origen humano, excepto sangre. (ISO 6717:2021).

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Označení normy:UNE EN ISO 6717:2022
Počet stran:22
Vydáno:2022-03-16
Status:Norma
Počet stran (Španělsky):23
DESCRIPTION

UNE EN ISO 6717:2022

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. It is not intended to cover specimen containers for forensic investigations. Examples of such specimens are, but not limited to, cerebral spinal fluid (CSF), faeces, infected bodily fluids, saliva, sperm, sputum, urine, tissue samples. Specimens and types of devices specifically excluded include specialized containers for cryopreservation, 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.

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