11.100 : Laboratory medicine

11.100.01

Laboratory medicine in general

11.100.10

In vitro diagnostic test systems

11.100.20

Biological evaluation of medical devices

11.100.30

Analysis of blood and urine

11.100.99

Other standards related to laboratory medicine
NBN EN ISO 23640:2013

NBN EN ISO 23640:2013

Superseded Historical

In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)

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CEN/TS 17390-2:2020

CEN/TS 17390-2:2020

Superseded Historical

Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood - Part 2: Isolated DNA

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CEN/TS 17390-3:2020

CEN/TS 17390-3:2020

Superseded Historical

Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood - Part 3: Preparations for analytical CTC staining

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CEN/TS 17305:2019

CEN/TS 17305:2019

Superseded Historical

Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for saliva - Isolated human DNA

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CEN/TS 17390-1:2020

CEN/TS 17390-1:2020

Superseded Historical

Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood - Part 1: Isolated RNA

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NBN EN ISO 7405:2009

NBN EN ISO 7405:2009

Superseded Historical

Dentistry - Evaluation of biocompatibility of medical devices used in dentistry (ISO 7405:2008)

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NBN EN ISO 10993-12:2008

NBN EN ISO 10993-12:2008

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Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2007)

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ISO 18113-1:2009 (R2015)

ISO 18113-1:2009 (R2015)

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In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) Part 1: Terms, definitions and general requirements

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ISO 18113-2:2009 (R2015)

ISO 18113-2:2009 (R2015)

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In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) Part 2: In vitro diagnostic reagents for professional use

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ISO 18113-3:2009 (R2015)

ISO 18113-3:2009 (R2015)

Superseded Historical

In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) Part 3: In vitro diagnostic instruments for professional use

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ISO 18113-4:2009 (R2015)

ISO 18113-4:2009 (R2015)

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In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) Part 4: In vitro diagnostic reagents for self-testing

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ISO 18113-5:2009 (R2015)

ISO 18113-5:2009 (R2015)

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In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) Part 5: In vitro diagnostic instruments for self-testing

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NBN EN 14254:2004

NBN EN 14254:2004

Superseded Historical

In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humans

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NBN EN ISO 17511:2003

NBN EN ISO 17511:2003

Superseded Historical

In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values assigned to calibrators and control materials (ISO 17511:2003)

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ASTM E1969-19

ASTM E1969-19

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Standard Practice for Microcrystal Testing in Forensic Analysis for Methamphetamine and Amphetamine

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