GBT 19703-2020: Certified reference materials and supporting documents for measurement of amounts of biogenic samples in in vitro diagnostic medical devices
GBT 19703-2020: Certified reference materials and supporting documents for measurement of amounts of biogenic samples in in vitro diagnostic medical devices, Total:26 items.
The international standard classification for "GBT 19703-2020: Certified reference materials and supporting documents for measurement of amounts of biogenic samples in in vitro diagnostic medical devices" includes: Medical equipment .
The Chinese standard classification for "GBT 19703-2020: Certified reference materials and supporting documents for measurement of amounts of biogenic samples in in vitro diagnostic medical devices" includes: Medical apparatus and devices in general , Sanitation in general .
国家市场监督管理总局、中国国家标准化管理委员会
- GB/T 19703-2020 In vitro diagnostic medical devices—Measurement of quantities in samples of biological origin—Requirements for certified reference materials and the content of supporting documentation
General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China
- GB/T 19703-2005 In vitro
- GB/T 19702-2005 In vitro
Professional Standard - Hygiene
- WS/T 253-2005 In vitro diagnostic medical devices-Measurement of quantities in samples of biological origin-Description of reference materials
GSO
- BH GSO ISO 15194:2017 In vitro diagnostic medical devices -- Measurement of quantities in samples of biological origin -- Requirements for certified reference materials and the content of supporting documentation
- OS GSO ISO 15194:2015 In vitro diagnostic medical devices -- Measurement of quantities in samples of biological origin -- Requirements for certified reference materials and the content of supporting documentation
- GSO ISO 15194:2015 In vitro diagnostic medical devices -- Measurement of quantities in samples of biological origin -- Requirements for certified reference materials and the content of supporting documentation
British Standards Institution (BSI)
- BS EN ISO 15194:2009(2016) In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Requirements for certified reference materials and the content of supporting documentation
German Institute for Standardization
- DIN EN ISO 15194:2009-10 In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for certified reference materials and the content of supporting documentation (ISO 15194:2009); German version EN ISO 15194:2009
SCC
- 07/30157023 DC BS EN ISO 15194. In vitro diagnostic medical devices. Measurement of quantities in samples of biological origin. Requirements for certified reference materials and the content of supporting documentation
- DANSK DS/EN ISO 15194:2009 In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for certified reference materials and the content of supporting documentation
- UNE-EN 12287:2000 In vitro diagnostic medical devices. Measurement of quantities in samples of biological origin. Description of reference materials.
- AENOR UNE-EN ISO 15194:2009 In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for certified reference materials and the content of supporting documentation (ISO 15194:2009)
- NS-EN ISO 15194:2009 In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Requirements for certified reference materials and the content of supporting documentation (ISO 15194:2009)
- UNE-EN 12286:1999 IN VITRO DIAGNOSTIC MEDICAL DEVICES. MEASUREMENT OF QUANTITIES IN SAMPLES OF BIOLOGICAL ORIGIN. PRESENTATION OF REFERENCE MEASUREMENT PROCEDURES.
- DIN EN ISO 15194 E:2007 Draft Document - In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for certified reference materials and the content of supporting documentation (ISO/DIS 15194:2007); German version prEN ISO ...
- NS-EN 12287:1999 In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Description of reference materials
Korean Agency for Technology and Standards (KATS)
- KS P ISO 15194-2019 In virto diagnostic medical devices — Measurement of quantities in samples of biological origin — Requirements for certified reference materials and the content of supporting documentation
- KS P ISO 15194-2014(2019) In virto diagnostic medical devices — Measurement of quantities in samples of biological origin — Requirements for certified reference materials and the content of supporting documentation
AENOR
- UNE-EN ISO 15194:2009 In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for certified reference materials and the content of supporting documentation (ISO 15194:2009)
DIN
- DIN EN 12287:1999 In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Description of reference materials
- DIN EN 12286:1999 In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Presentation of reference measurement procedures
CEN - European Committee for Standardization
- EN 12287:1999 In Vitro Diagnostic Medical Devices - Measurement of Quantities in Samples of Biological Origin - Description of Reference Materials
RU-GOST R
- GOST R ISO 15194-2013 In vitro diagnostic medical devices. Measurement of quantities in samples of biological origin. Requirements for certified reference materials and the content of supporting documentation
Association Francaise de Normalisation
- NF EN ISO 15194:2009 In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for certified reference materials and the content of associated documentation
International Organization for Standardization (ISO)
- ISO/DIS 15194:2024 In vitro diagnostic medical devices — Requirements for certified reference materials and the content of supporting documentation