11.100.10:In vitro diagnostic test systems
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BS 06/30146511 DC
This document has been replaced. View the most recent version.
BS ISO 18113-1. Clinical laboratory testing and in vitro diagnostic medical systems. Information supplied by the manufacturer (labelling). Part 1. Terms, definitions and general requirements
standard by BSI Group, 12/07/2006.
Languages:
Historical Editions: BS EN ISO 18113-1:2024, BS EN ISO 18113-1:2011, BS EN ISO 18113-1:2009
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BS 06/30146515 DC
This document has been replaced. View the most recent version.
BS ISO 18113-2. Clinical laboratory testing and in vitro diagnostic medical systems. Information supplied by the manufacturer (labelling). Part 2. In vitro diagnostic reagents for professional use
standard by BSI Group, 12/07/2006.
Languages:
Historical Editions: BS EN ISO 18113-2:2024, BS EN ISO 18113-2:2011, BS EN ISO 18113-2:2009, BS EN 375:2001, BS EN 375:1992
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BS 06/30146518 DC
This document has been replaced. View the most recent version.
BS ISO 18113-3. Clinical laboratory testing and in vitro diagnostic medical systems. Information supplied by the manufacturer (labelling). Part 3. In vitro diagnostic instruments for professional use
standard by BSI Group, 12/07/2006.
Languages:
Historical Editions: BS EN ISO 18113-3:2024, BS EN ISO 18113-3:2011, BS EN ISO 18113-3:2009, BS EN 591:2001, BS EN 591:1995
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BS 06/30146522 DC
This document has been replaced. View the most recent version.
BS ISO 18113-4. Clinical laboratory testing and in vitro diagnostic medical systems. Information supplied by the manufacturer (labelling). Part 4. In vitro diagnostic reagents for self-testing
standard by BSI Group, 12/07/2006.
Languages:
Historical Editions: BS EN ISO 18113-4:2024, BS EN ISO 18113-4:2011, BS EN ISO 18113-4:2009, BS EN 376:2002, BS EN 376:1992
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BS 06/30146526 DC
This document has been replaced. View the most recent version.
BS ISO 18113-5. Clinical laboratory testing and in vitro diagnostic medical systems. Information supplied by the manufacturer (labelling). Part 5. In vitro diagnostic instruments for self-testing
standard by BSI Group, 12/07/2006.
Languages:
Historical Editions: BS EN ISO 18113-5:2024, BS EN ISO 18113-5:2011, BS EN ISO 18113-5:2009, BS EN 592:2002, BS EN 592:1995
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BS 06/30154803 DC
EN ISO 15193. In vitro diagnostic medical devices. Measurement of quantities in samples of biological origin. Requirements for content and presentation of reference measurement procedures
standard by BSI Group, 08/16/2006.
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BS 09/30175345 DC
BS EN ISO 29701. Nanotechnologies. Endotoxin test on nanomaterial samples for in vitro systems. Limulus amebocyte lysate (LAL) test
standard by BSI Group, 06/05/2009.
Languages:
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BS 09/30210157 DC
This document has been replaced. View the most recent version.
BS EN ISO 23640. In vitro diagnostic medical devices. Stability testing of in vitro diagnostic reagents
standard by BSI Group, 12/02/2009.
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Historical Editions: BS EN ISO 23640:2015, BS EN ISO 23640:2013, BS EN ISO 23640:2011, BS EN 13640:2002
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BS 10/30216029 DC
This document has been replaced. View the most recent version.
BS EN 61326-2-6. Electrical equipment for measurement, control and laboratory use . EMC requirements. Part 2-6. Particular requirements. In vitro diagnostic (IVD) medical equipment
standard by BSI Group, 01/25/2010.
Languages:
Historical Editions: BS EN IEC 61326-2-6:2021, BS EN 61326-2-6:2013, BS EN 61326-2-6:2006, BS EN 60205:2006+A1:2009, BS EN 60205:2006, BS EN 61326:1998, BS EN 60205:2001, BS 6454:1983
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BS 10/30219700 DC
This document has been replaced. View the most recent version.
BS ISO 13079. Laboratory glass and plastics ware. Tubes and support for the measurement of erythrocytic sedimentation rate by the Westergren method
standard by BSI Group, 04/19/2010.
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Historical Editions: BS EN ISO 13079:2011, BS 2554:1987, BS 2554:1968