In vitro diagnostic medical devices. Single-use receptacles for the collection of specimens, other than blood, from humans Ingestion-build-126766 test report

test report

has been reduced to one

manufacture and final check is specified in the clauses and paragraphs of ISO 5167:2003 (parts 2 to 4)

General requirements and general requirements for tests

Information security risk assessment

In vitro diagnostic medical devices. Single-use receptacles for the collection of specimens, other than blood, from humans Ingestion-build-126766 test reportBS EN 14254: 2004 specifies requirements and test methods for single use evacuated and non evacuated receptacles, 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. NOTE 1 Requirements and test methods for evacuated and non evacuated single use venous blood specimen containers are specified in EN 14820.