DIN EN ISO 6717:2021
In vitro diagnostic medical devices - Single-use containers for the collection of specimens from humans other than blood (ISO 6717:2021); German version EN ISO 6717:2021
- Standard No.
- DIN EN ISO 6717:2021
- Release Date
- 2021
- Published By
- German Institute for Standardization
- Status
- 2020-09
- Replace By
- DIN EN 14254:2004
- DIN EN ISO 6717:2020
- DIN EN ISO 6717:2021-12
- Latest
- DIN EN ISO 6717:2021
- DIN EN ISO 6717:2020
- DIN EN ISO 6717:2021-12
- 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 pu
DIN EN ISO 6717:2021 history
- 2021 DIN EN ISO 6717:2021 In vitro diagnostic medical devices - Single-use containers for the collection of specimens from humans other than blood (ISO 6717:2021); German version EN ISO 6717:2021
- 2020 DIN EN ISO 6717:2020 In vitro diagnostic medical devices - Single-use containers for the collection of specimens, other than blood, from humans (ISO/DIS 6717:2020); German and English version prEN ISO 6717:2020
- 2004 DIN EN 14254:2004 In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humans; German version EN 14254:2004
DIN EN ISO 6717:2021 In vitro diagnostic medical devices - Single-use containers for the collection of specimens from humans other than blood (ISO 6717:2021); German version EN ISO 6717:2021 was changed to DIN EN 14254:2004 In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humans; German version EN 14254:2004.
