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SN EN 724
Guidance on the application of EN 29001 and EN 46001 and of EN 29002 and EN 46002 for non-active medical devices
Edition
1995
OEVE EN 61223-2-4
Evaluation and routine testing in medical imaging departments - Part 2-4: Constancy tests - Hard copy cameras
Edition
1994-11
GA S98-130
Sterilisation of medical devices - Interpretation guide for NF EN 554 intended for health establishments - Validation and routine inspection for steam sterilisation (October 1994)
Edition
2002-05-01
OENORM EN ISO 18153
In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values for catalytic concentration of enzymes assigned to calibrators and control materials (ISO 18153:2003)
Edition
2003-11-01
OENORM EN 14079
Non-active medical devices - Performance requirements and test methods for absorbent cotton gauze and absorbent cotton and viscose gauze
Edition
2003-07-01
OEVE EN 50103
Guidance on the application of EN 29001 and EN 46001 and of EN 29002 and EN 46002 for the active (including active implantable) medical device industry
Edition
1995-10-04
OEVE EN 61220
Ultrasonics - Fields - Guidance for the measurement and characterization of ultrasonic fields generated by medical ultrasonic equipment using hydrophones in the ......(abbreviated)
Edition
1996-06-20
OENORM EN ISO 10993-4
Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2017)
Edition
2018-01-01
OENORM EN ISO 10993-16
Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2017)
Edition
2018-01-15
OENORM EN ISO 10524-1
Pressure regulators for use with medical gases - Part 1: Pressure regulators and pressure regulators with flow-metering devices (ISO 10524-1:2018)
Edition
2019-07-15