UNE-EN ISO 6717:2022
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 (ISO 6717:2021)
Hardcopy , PDF
Spanish, Castilian, English
16-03-2022
This document specifies requirements and test methods for specialized single-use evacuated and nonevacuatedcontainers, intended by their manufacturers, for the primary containment and preservationof specimens, other than blood specimens, derived from the human body, for the purposes of in vitrodiagnostic 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 bodilyfluids, 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 bloodspecimen collection containers are specified in ISO 6710.This document does not specify requirements for auxiliary devices used in conjunction with specimencontainers.
| Committee |
CTN 129
|
| DocumentType |
Standard
|
| Pages |
23
|
| PublisherName |
Asociación Española de Normalización
|
| Status |
Current
|
| Standards | Relationship |
| ISO 6717:2021 | Identical |
| EN ISO 6717:2021 | Identical |
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