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CAN/CSA-C22.2 No. 60601-2-34-12
Medical electrical equipment - Part 2-34: Particular requirements for the basic safety and essential performance of invasive blood pressure monitoring equipment
Edition
2012-06-01
CAN/CSA-ISO 15197
In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (Adopted ISO 15197:2013, second edition, 2013-05-15)
Edition
2015-08-01
CAN/CSA-Z902
Blood and blood components
Edition
2025-03-01
CSA ISO 8637-1
Extracorporeal systems for blood purification - Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (Adopted ISO 8637-1:2017, first edition, 2017-11)
Edition
2021-08-01
CSA ISO 8637-2
Extracorporeal systems for blood purification - Part 2: Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters (Adopted ISO 8637-2:2018, first edition, 2018-07)
Edition
2021-08-01
CSA ISO 20186-1
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1: Isolated cellular RNA (Adopted ISO 20186-1:2019, first edition, 2019-02)
Edition
2022-08-01
CSA ISO 20186-2
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2: Isolated genomic DNA (Adopted ISO 20186-2:2019, first edition, 2019-02)
Edition
2022-08-01
CSA ISO 20186-3
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 3: Isolated circulating cell free DNA from plasma (Adopted ISO 20186-3:2019, first edition, 2019-09)
Edition
2022-08-01
OENORM ENV 13730-1
Health informatics - Blood transfusion related messages - Part 1: Subject of care related messages
Edition
2002-03-01
OENORM ENV 13730-2
Healthcare Informatics - Blood transfusion related messages - Part 2: Production related messages (BTR-PROD)
Edition
2003-01-01