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Homepage>BSI Standards>11 ZDRAVOTNÍ TECHNIKA>11.100 Laboratorní lékařství>11.100.10 Systémy diagnostických zkoušek in vitro

11.100.10 Systémy diagnostických zkoušek in vitro

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77 results
First page12467Last page
BS EN ISO 20166-1:2018
Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for formalin-fixed and paraffin-embedded (FFPE) tissue Isolated RNA
Vydáno: 2019-02-22
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BS EN ISO 17511:2021 - TC
Tracked Changes. In vitro diagnostic medical devices. Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples
Vydáno: 2021-12-10
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BS EN ISO 4307:2021
Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for saliva. Isolated human DNA
Vydáno: 2021-11-04
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BS EN ISO 20166-4:2021
Molecular in vitro diagnostic examinations. Specifications for preexamination processes for formalin-fixed and paraffin-embedded (FFPE) tissue In situ detection techniques
Vydáno: 2021-07-28
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BS EN IEC 61326-2-6:2021 - TC
Tracked Changes. Electrical equipment for measurement, control and laboratory use. EMC requirements Particular requirements. In vitro diagnostic (IVD) medical equipment
Vydáno: 2021-11-10
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PD CEN/TS 17742:2022
Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for venous whole blood. Isolated circulating cell free RNA from plasma
Vydáno: 2022-05-11
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PD CEN ISO/TS 7552-1:2024
Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for circulating tumour cells (CTCs) in venous whole blood Isolated RNA
Vydáno: 2024-11-14
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BS EN ISO 18113-1:2024
In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling) Terms, definitions, and general requirements
Vydáno: 2024-06-12
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BS EN ISO 18113-1:2024 - TC
Tracked Changes. In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling) Terms, definitions, and general requirements
Vydáno: 2024-06-14
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BS EN ISO 15194:2009
In vitro diagnostic medical devices. Measurement of quantities in samples of biological origin. Requirements for certified reference materials and the content of supporting documentation
Vydáno: 2016-01-31
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BS EN ISO 17511:2021
In vitro diagnostic medical devices. Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples
Vydáno: 2021-06-07
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PD CEN/TS 17688-1:2021
Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for Fine Needle Aspirates (FNAs) Isolated cellular RNA
Vydáno: 2021-12-23
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77 results
First page12467Last page