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

Information security risk assessment

especially those that are new

This European Standard specifies requirements and describes test methods for odorizing devices for CO2 low pressure systems which release an odorizing substance into the extinguishant during discharge

Methods of determining the replacement period

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