11.100 : Laboratory medicine
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DIN EN ISO 10993-4/A1:2024-04
Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood - Amendment 1 (ISO 10993-4:2017/DAM 1:2024), German and English version EN ISO 10993-4:2017/prA1:2024
4/1/2024 - PDF - English, German - DIN
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DIN EN ISO 7405:2024-04
Dentistry - Evaluation of biocompatibility of medical devices used in dentistry (ISO/DIS 7405:2024), German and English version prEN ISO 7405:2024
4/1/2024 - PDF - English, German - DIN
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DIN 58987:2024-04
Haemostaseology - Reference method for the Von Willebrand Factor antigen, Text in German and English
4/1/2024 - PDF - English, German - DIN
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DIN 58988:2024-04
Haemostaseology - Reference method for the Von Willebrand Factor multimers, Text in German and English
4/1/2024 - PDF - English, German - DIN
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DIN EN ISO 15194:2024-02
In vitro diagnostic medical devices - Requirements for certified reference materials and the content of supporting documentation (ISO/DIS 15194:2023), German and English version prEN ISO 15194:2023
2/1/2024 - PDF - English, German - DIN
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DIN EN ISO 15193:2024-02
In vitro diagnostic medical devices - Requirements for reference measurement procedures (ISO/DIS 15193:2023), German and English version prEN ISO 15193:2023
2/1/2024 - PDF - English, German - DIN
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DIN EN ISO 5649:2024-02
Medical laboratories - Concepts and specifications for the design, development, implementation, and use of laboratory-developed tests (ISO/DIS 5649:2023), German and English version prEN ISO 5649:2023
2/1/2024 - PDF - English, German - DIN
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DIN EN ISO 10993-17:2024-02
Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents (ISO 10993-17:2023), German version EN ISO 10993-17:2023
2/1/2024 - PDF - German - DIN
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DIN 58932-3:2024-02
Haematology - Determination of the concentration of blood corpuscles in blood - Part 3: Reference method for the determination of the concentration of erythrocytes, Text in German and English
2/1/2024 - PDF - English, German - DIN
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DIN EN ISO 10993-18:2023-11
Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020 + Amd 1:2022), German version EN ISO 10993-18:2020 + A1:2023
11/1/2023 - PDF - German - DIN
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DIN 58932-1:2023-08
Haematology - Determination of the concentration of blood corpuscles in blood - Part 1: Blood collection, sample preparation, influence quantities, interference factors, Text in German and English
8/1/2023 - PDF - English, German - DIN
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DIN EN ISO 10993-15:2023-07
Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2019), German version EN ISO 10993-15:2023
7/1/2023 - PDF - German - DIN
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DIN EN ISO 10993-10:2023-04
Biological evaluation of medical devices - Part 10: Tests for skin sensitization (ISO 10993-10:2021), German version EN ISO 10993-10:2023
4/1/2023 - PDF - German - DIN
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DIN CEN ISO/TS 5798:2023-03
In vitro diagnostic test systems - Requirements and recommendations for detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) by nucleic acid amplification methods (ISO/TS 5798:2022), German version CEN ISO/TS 5798:2022
3/1/2023 - PDF - German - DIN
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DIN EN ISO 15189:2023-03
Medical laboratories - Requirements for quality and competence (ISO 15189:2022), German version EN ISO 15189:2022
3/1/2023 - PDF - German - DIN
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DIN ISO 4802-1:2023-03
Glassware - Hydrolytic resistance of the interior surfaces of glass containers - Part 1: Determination by titration method and classification (ISO/DIS 4802-1:2022), Text in German and English
3/1/2023 - PDF - English, German - DIN
Learn More€79.72 -
DIN ISO 4802-2:2023-03
Glassware - Hydrolytic resistance of the interior surfaces of glass containers - Part 2: Determination by flame spectrometry and classification (ISO/DIS 4802-2:2022), Text in German and English
3/1/2023 - PDF - English, German - DIN
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DIN EN ISO 10993-2:2023-02
Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO 10993-2:2022), German version EN ISO 10993-2:2022
2/1/2023 - PDF - German - DIN
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DIN EN ISO 10993-7:2022-09
Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2008 + Cor 1:2009 + Amd 1:2019), German version EN ISO 10993-7:2008 + AC:2009 + A1:2022
9/1/2022 - PDF - German - DIN
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DIN CEN/TS 17747:2022-08
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for exosomes and other extracellular vesicles in venous whole blood - DNA, RNA and proteins, German version CEN/TS 17747:2022
8/1/2022 - PDF - German - DIN
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DIN CEN/TS 17811:2022-08
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for urine and other body fluids - Isolated cell free DNA, German version CEN/TS 17811:2022
8/1/2022 - PDF - German - DIN
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DIN EN ISO 24443:2022-08
Cosmetics - Determination of sunscreen UVA photoprotection in vitro (ISO 24443:2021, Corrected version 2022-02), German version EN ISO 24443:2021
8/1/2022 - PDF - German - DIN
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DIN CEN/TS 17688-3:2022-07
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for Fine Needle Aspirates (FNAs) - Part 3: Isolated genomic DNA, German version CEN/TS 17688-3:2021
7/1/2022 - PDF - German - DIN
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DIN CEN/TS 17742:2022-07
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free RNA from plasma, German version CEN/TS 17742:2022
7/1/2022 - PDF - German - DIN
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DIN CEN/TS 17688-2:2022-06
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for Fine Needle Aspirates (FNAs) - Part 2: Isolated proteins, German version CEN/TS 17688-2:2021
6/1/2022 - PDF - German - DIN
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DIN CEN/TS 17688-1:2022-06
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for Fine Needle Aspirates (FNAs) - Part 1: Isolated cellular RNA, German version CEN/TS 17688-1:2021
6/1/2022 - PDF - German - DIN
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DIN 58923:2022-05
Haemostaseology - Reference method for the ristocetin-cofactor activity of the VWF, Text in German and English
5/1/2022 - PDF - English, German - DIN
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DIN 58924:2022-05
Haemostaseology - Reference method for the determination of the collagen binding acitvity of the VWF, Text in German and English
5/1/2022 - PDF - English, German - DIN
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DIN EN ISO 20776-2:2022-04
Clinical laboratory testing and in vitro diagnostic test systems - Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices - Part 2: Evaluation of performance of antimicrobial susceptibility test devices against reference broth micro-dilution (ISO 20776-2:2021), German version EN ISO 20776-2:2022
4/1/2022 - PDF - German - DIN
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DIN EN ISO 10993-9:2022-03
Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:2019), German version EN ISO 10993-9:2021
3/1/2022 - PDF - German - DIN
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DIN EN ISO 4307:2022-02
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for saliva - Isolated human DNA (ISO 4307:2021), German version EN ISO 4307:2021
2/1/2022 - PDF - German - DIN
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DIN EN ISO 16256:2022-02
Clinical laboratory testing and in vitro diagnostic test systems - Broth micro-dilution reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseases (ISO 16256:2021), German version EN ISO 16256:2021
2/1/2022 - PDF - German - DIN
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DIN CEN/TS 17626:2022-01
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for human specimen - Isolated microbiome DNA, German version CEN/TS 17626:2021
1/1/2022 - PDF - German - DIN
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DIN EN ISO 6717:2021-12
In vitro diagnostic medical devices - Single-use containers for the collection of specimens from humans other than blood (ISO 6717:2021), German version EN ISO 6717:2021
12/1/2021 - PDF - German - DIN
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DIN EN ISO 17511:2021-11
In vitro diagnostic medical devices - Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples (ISO 17511:2020), German version EN ISO 17511:2021
11/1/2021 - PDF - German - DIN
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DIN EN ISO 20184-3:2021-11
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for frozen tissue - Part 3: Isolated DNA (ISO 20184-3:2021), German version EN ISO 20184-3:2021
11/1/2021 - PDF - German - DIN
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DIN EN ISO 20166-4:2021-11
Molecular in vitro diagnostic examinations - Specifications for preexamination processes for formalin-fixed and paraffin-embedded (FFPE) tissue - Part 4: In situ detection techniques (ISO 20166-4:2021), German version EN ISO 20166-4:2021
11/1/2021 - PDF - German - DIN
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DIN 58912-1:2021-11
Haemostaseology - Determination of the antithrombin activity - Part 1: Reference measurement procedure using a synthetic peptide substrate, Text in German and English
11/1/2021 - PDF - English, German - DIN
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DIN EN ISO 23162:2021-10
Basic semen examination - Specification and test methods (ISO 23162:2021), German version EN ISO 23162:2021
10/1/2021 - PDF - German - DIN
Learn More€110.00 -
DIN EN ISO 10993-23:2021-10
Biological evaluation of medical devices - Part 23: Tests for irritation (ISO 10993-23:2021), German version EN ISO 10993-23:2021
10/1/2021 - PDF - German - DIN
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DIN EN ISO 18113-1:2021-09
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO/DIS 18113-1:2021), German and English version prEN ISO 18113-1:2021
9/1/2021 - PDF - English, German - DIN
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DIN EN ISO 18113-2:2021-09
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO/DIS 18113-2:2021), German and English version prEN ISO 18113-2:2021
9/1/2021 - PDF - English, German - DIN
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DIN EN ISO 18113-3:2021-09
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO/DIS 18113-3:2021), German and English version prEN ISO 18113-3:2021
9/1/2021 - PDF - English, German - DIN
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DIN EN ISO 18113-4:2021-09
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO/DIS 18113-4:2021), German and English version prEN ISO 18113-4:2021
9/1/2021 - PDF - English, German - DIN
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DIN EN ISO 18113-5:2021-09
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO/DIS 18113-5:2021), German and English version prEN ISO 18113-5:2021
9/1/2021 - PDF - English, German - DIN
Learn More€72.80 -
DIN 58931:2021-09
Haematology - Determination of haemoglobin concentration in blood - Reference method, Text in German and English
9/1/2021 - PDF - English, German - DIN
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DIN EN ISO 23118:2021-08
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma (ISO 23118:2021), German version EN ISO 23118:2021
8/1/2021 - PDF - German - DIN
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DIN EN ISO 10993-12:2021-08
Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2021), German version EN ISO 10993-12:2021
8/1/2021 - PDF - German - DIN
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DIN EN ISO 22442-1:2021-08
Medical devices utilizing animal tissues and their derivatives - Part 1: Application of risk management (ISO 22442-1:2020), German version EN ISO 22442-1:2020.
8/1/2021 - PDF - German - DIN
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DIN 58932-6:2021-08
Haematology - Determination of the concentration of blood corpuscles in blood - Part 6: Reference method for the determination of the concentration of CD4 positive lymphocytes, Text in German and English
8/1/2021 - PDF - English, German - DIN
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DIN EN ISO 20916:2021-05
In vitro diagnostic medical devices - Clinical performance studies using specimens from human subjects - Good study practice (ISO 20916:2019), German and English version prEN ISO 20916:2021
5/1/2021 - PDF - English, German - DIN
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DIN EN ISO 10993-1:2021-05
Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2018, including corrected version 2018-10), German version EN ISO 10993-1:2020
5/1/2021 - PDF - German - DIN
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DIN EN ISO 14155:2021-05
Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020), German version EN ISO 14155:2020
5/1/2021 - PDF - German - DIN
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DIN EN ISO 22442-2:2021-04
Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling (ISO 22442-2:2020), German version EN ISO 22442-2:2020
4/1/2021 - PDF - German - DIN
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DIN EN ISO 20776-1:2020-12
Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices - Part 1: Broth micro-dilution reference method for testing the in vitro activity of antimicrobial agents against rapidly growing aerobic bacteria involved in infectious diseases (ISO 20776-1:2019, including Corrected version 2019-12), German version EN ISO 20776-1:2020
12/1/2020 - PDF - German - DIN
Learn More€85.79 -
DIN EN ISO 22367:2020-09
Medical laboratories - Application of risk management to medical laboratories (ISO 22367:2020), German version EN ISO 22367:2020
9/1/2020 - PDF - German - DIN
Learn More€201.96 -
DIN CEN/TS 17390-1:2020-05
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood - Part 1: Isolated RNA, German version CEN/TS 17390-1:2020
5/1/2020 - PDF - German - DIN
Learn More€73.93 -
DIN CEN/TS 17390-3:2020-05
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, German version CEN/TS 17390-3:2020
5/1/2020 - PDF - German - DIN
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DIN CEN/TS 17390-2:2020-05
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood - Part 2: Isolated DNA, German version CEN/TS 17390-2:2020
5/1/2020 - PDF - German - DIN
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DIN EN ISO 20186-3:2020-04
Molecular in-vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 3: Isolated circulating cell free DNA from plasma (ISO 20186-3:2019), German version EN ISO 20186-3:2019
4/1/2020 - PDF - German - DIN
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DIN 58903:2020-04
Haemostaseology - Deficient plasma - Requirements, preparation, Text in German and English
4/1/2020 - PDF - English, German - DIN
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DIN 58909-1:2020-04
Haemostaseology - Determination of factor VIII coagulant activity (FVIII:C) - Part 1: Reference measurement procedure for the one-stage method, Text in German and English
4/1/2020 - PDF - English, German - DIN
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DIN 58909-2:2020-04
Haemostaseology - Determination of factor VIII coagulant activity (FVIII:C) - Part 2: Reference measurement procedure using a synthetic peptide substrate, Text in German and English
4/1/2020 - PDF - English, German - DIN
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DIN EN ISO 20186-1:2019-08
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1: Isolated cellular RNA (ISO 20186-1:2019), German version EN ISO 20186-1:2019
8/1/2019 - PDF - German - DIN
Learn More€92.62 -
DIN EN ISO 20186-2:2019-08
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2: Isolated genomic DNA (ISO 20186-2:2019), German version EN ISO 20186-2:2019
8/1/2019 - PDF - German - DIN
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DIN EN ISO 15195:2019-07
Laboratory medicine - Requirements for the competence of calibration laboratories using reference measurement procedures (ISO 15195:2018), German version EN ISO 15195:2019
7/1/2019 - PDF - German - DIN
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DIN EN ISO 20184-2:2019-06
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for frozen tissue - Part 2: Isolated proteins (ISO 20184-2:2018), German version EN ISO 20184-2:2018
6/1/2019 - PDF - German - DIN
Learn More€85.79 -
DIN EN ISO 20184-1:2019-06
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for frozen tissue - Part 1: Isolated RNA (ISO 20184-1:2018), German version EN ISO 20184-1:2018
6/1/2019 - PDF - German - DIN
Learn More€92.62 -
DIN EN ISO 20166-1:2019-04
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for formalin-fixed and paraffin-embedded (FFPE) tissue - Part 1: Isolated RNA (ISO 20166-1:2018), German version EN ISO 20166-1:2018
4/1/2019 - PDF - German - DIN
Learn More€99.35 -
DIN EN ISO 20166-2:2019-04
Molecular in vitro diagnostic examinations - Specifications for pre-examinations processes for formalin-fixed and paraffin-embedded (FFPE) tissue - Part 2: Isolated proteins (ISO 20166-2:2018), German version EN ISO 20166-2:2018
4/1/2019 - PDF - German - DIN
Learn More€92.62 -
DIN EN ISO 20166-3:2019-04
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for formalin-fixed and paraffin-embedded (FFPE) tissue - Part 3: Isolated DNA (ISO 20166-3:2018), German version EN ISO 20166-3:2019
4/1/2019 - PDF - German - DIN
Learn More€85.79 -
DIN EN ISO 7405:2019-03
Dentistry - Evaluation of biocompatibility of medical devices used in dentistry (ISO 7405:2018, Corrected version 2018-12), German version EN ISO 7405:2018
3/1/2019 - PDF - German - DIN
Learn More€126.26 -
DIN 58989:2018-10
Haemostaseology - HPLC-MS methods for the quantification of direct oral anticoagulants (DOAC) - Rivaroxaban, Text in German and English
10/1/2018 - PDF - English, German - DIN
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DIN EN ISO 10993-11:2018-09
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2017)
9/1/2018 - PDF - English - DIN
Learn More€150.93 -
DIN EN ISO 10993-11:2018-09
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2017), German version EN ISO 10993-11:2018
9/1/2018 - PDF - German - DIN
Learn More€120.84 -
DIN EN ISO 10993-16:2018-02
Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2017)
2/1/2018 - PDF - English - DIN
Learn More€107.48 -
DIN EN ISO 10993-16:2018-02
Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2017), German version EN ISO 10993-16:2017
2/1/2018 - PDF - German - DIN
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DIN EN ISO 10993-4:2017-12
Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2017)
12/1/2017 - PDF - English - DIN
Learn More€230.75 -
DIN EN ISO 10993-4:2017-12
Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2017), German version EN ISO 10993-4:2017
12/1/2017 - PDF - German - DIN
Learn More€184.58 -
DIN EN ISO 10993-6:2017-09
Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2016)
9/1/2017 - PDF - English - DIN
Learn More€144.02 -
DIN EN ISO 10993-6:2017-09
Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2016), German version EN ISO 10993-6:2016
9/1/2017 - PDF - German - DIN
Learn More€115.33 -
DIN 12980:2017-05
Laboratory installations - Safety cabinets and glove boxes for cytotoxic substances and other CMR drugs.
5/1/2017 - PDF - German - DIN
Learn More€92.62 -
DIN ISO 4802-1:2017-02
Glassware - Hydrolytic resistance of the interior surfaces of glass containers - Part 1: Determination by titration method and classification (ISO 4802-1:2016)
2/1/2017 - PDF - English - DIN
Learn More€91.12 -
DIN ISO 4802-2:2017-02
Glassware - Hydrolytic resistance of the interior surfaces of glass containers - Part 2: Determination by flame spectrometry and classification (ISO 4802-2:2016)
2/1/2017 - PDF - English - DIN
Learn More€91.12 -
DIN ISO 4802-1:2017-02
Glassware - Hydrolytic resistance of the interior surfaces of glass containers - Part 1: Determination by titration method and classification (ISO 4802-1:2016)
2/1/2017 - PDF - German - DIN
Learn More€72.80 -
DIN ISO 4802-2:2017-02
Glassware - Hydrolytic resistance of the interior surfaces of glass containers - Part 2: Determination by flame spectrometry and classification (ISO 4802-2:2016)
2/1/2017 - PDF - German - DIN
Learn More€72.80 -
DIN 58905-1:2016-12
Haemostaseology - Blood collection - Part 1: Preparation of plasma from citrated venous blood for coagulation testing, Text in German and English
12/1/2016 - PDF - English, German - DIN
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DIN 58910-1:2016-02
Haemostaseology - Determination of thromboplastin (prothrombin) time - Part 1: Reference measurement procedure for the determination in plasma from citrated venous blood, Text in German and English
2/1/2016 - PDF - English, German - DIN
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DIN EN ISO 23640:2015-12
In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011), German version EN ISO 23640:2015.
12/1/2015 - PDF - German - DIN
Learn More€65.89 -
DIN EN ISO 23640:2015-12
In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)
12/1/2015 - PDF - English - DIN
Learn More€82.52 -
DIN EN ISO 15197:2015-12
In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2013), German version EN ISO 15197:2015.
12/1/2015 - PDF - German - DIN
Learn More€136.82 -
DIN EN ISO 15197:2015-12
In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2013)
12/1/2015 - PDF - English - DIN
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DIN 58964:2015-09
Quality assurance of POCT results - Assessment criteria for comparison measurement and implementation
9/1/2015 - PDF - German - DIN
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DIN 58964:2015-09
Quality assurance of POCT results - Assessment criteria for comparison measurement and implementation
9/1/2015 - PDF - English - DIN
Learn More€82.52 -
DIN 58908:2015-09
Haemostaseology - Determination of activated partial thromboplastin time (APTT) - Reference measurement procedure, Text in German and English
9/1/2015 - PDF - English, German - DIN
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DIN EN ISO 10993-3:2015-02
Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:2014), German version EN ISO 10993-3:2014
2/1/2015 - PDF - German - DIN
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DIN EN ISO 10993-3:2015-02
Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:2014)
2/1/2015 - PDF - English - DIN
Learn More€144.02 -
DIN ISO 13022:2014-06
Medical products containing viable human cells - Application of risk management and requirements for processing practices (ISO 13022:2012)
6/1/2014 - PDF - German - DIN
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DIN ISO 13022:2014-06
Medical products containing viable human cells - Application of risk management and requirements for processing practices (ISO 13022:2012)
6/1/2014 - PDF - English - DIN
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DIN EN ISO 19001:2013-07
In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology (ISO 19001:2013), German version EN ISO 19001:2013.
7/1/2013 - PDF - German - DIN
Learn More€79.72 -
DIN EN ISO 19001:2013-07
In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology (ISO 19001:2013)
7/1/2013 - PDF - English - DIN
Learn More€99.44 -
€68.60
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€85.98
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DIN EN ISO 18113-2:2013-01
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009)
1/1/2013 - PDF - English - DIN
Learn More€91.12 -
DIN EN ISO 18113-3:2013-01
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009)
1/1/2013 - PDF - English - DIN
Learn More€91.12 -
DIN EN ISO 18113-4:2013-01
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009)
1/1/2013 - PDF - English - DIN
Learn More€91.12 -
DIN EN ISO 18113-5:2013-01
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009)
1/1/2013 - PDF - English - DIN
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DIN EN ISO 18113-1:2013-01
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)
1/1/2013 - PDF - English - DIN
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DIN EN ISO 18113-2:2013-01
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009), German version EN ISO 18113-2:2011.
1/1/2013 - PDF - German - DIN
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DIN EN ISO 18113-3:2013-01
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009), German version EN ISO 18113-3:2011.
1/1/2013 - PDF - German - DIN
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DIN EN ISO 18113-4:2013-01
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009), German version EN ISO 18113-4:2011.
1/1/2013 - PDF - German - DIN
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DIN EN ISO 18113-5:2013-01
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009), German version EN ISO 18113-5:2011.
1/1/2013 - PDF - German - DIN
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DIN EN ISO 18113-1:2013-01
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009), German version EN ISO 18113-1:2011.
1/1/2013 - PDF - German - DIN
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DIN EN ISO 29701:2011-01
Nanotechnologies - Endotoxin test on nanomaterial samples for in vitro systems - Limulus amebocyte lysate (LAL) test (ISO 29701:2010), German version EN ISO 29701:2010
1/1/2011 - PDF - German - DIN
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DIN EN ISO 29701:2011-01
Nanotechnologies - Endotoxin test on nanomaterial samples for in vitro systems - Limulus amebocyte lysate (LAL) test (ISO 29701:2010)
1/1/2011 - PDF - English - DIN
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DIN EN ISO 10993-13:2010-11
Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:2010), German version EN ISO 10993-13:2010
11/1/2010 - PDF - German - DIN
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DIN EN ISO 10993-13:2010-11
Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:2010)
11/1/2010 - PDF - English - DIN
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DIN EN ISO 15193:2009-10
In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for content and presentation of reference measurement procedures (ISO 15193:2009); German version EN ISO 15193:2009
10/1/2009 - PDF - German - DIN
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DIN EN ISO 15193:2009-10
In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for content and presentation of reference measurement procedures (ISO 15193:2009); German version EN ISO 15193:2009
10/1/2009 - PDF - English - DIN
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DIN EN ISO 15194:2009-10
In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for certified reference materials and the content of supporting documentation (ISO 15194:2009); German version EN ISO 15194:2009
10/1/2009 - PDF - German - DIN
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DIN EN ISO 15194:2009-10
In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for certified reference materials and the content of supporting documentation (ISO 15194:2009); German version EN ISO 15194:2009
10/1/2009 - PDF - English - DIN
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DIN EN ISO 10993-5:2009-10
Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009), German version EN ISO 10993-5:2009
10/1/2009 - PDF - German - DIN
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DIN EN ISO 10993-5:2009-10
Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009)
10/1/2009 - PDF - English - DIN
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DIN EN ISO 10993-14:2009-08
Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001), German version EN ISO 10993-14:2009.
8/1/2009 - PDF - German - DIN
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DIN EN ISO 10993-14:2009-08
Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001)
8/1/2009 - PDF - English - DIN
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DIN EN ISO 22442-3:2008-03
Medical devices utilizing animal tissues and their derivatives - Part 3: Validation of the elimination and/or inactivation of viruses and transmissible spongiform encephalopathy (TSE) agents (ISO 22442-3:2007); German version EN ISO 22442-3:2007
3/1/2008 - PDF - German - DIN
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DIN EN ISO 22442-3:2008-03
Medical devices utilizing animal tissues and their derivatives - Part 3: Validation of the elimination and/or inactivation of viruses and transmissible spongiform encephalopathy (TSE) agents (ISO 22442-3:2007); German version EN ISO 22442-3:2007
3/1/2008 - PDF - English - DIN
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DIN 58932-5:2007-10
Haematology - Determination of the concentration of blood corpuscles in blood - Part 5: Reference method for the determination of the concentration of thrombocytes; Text in German and English
10/1/2007 - PDF - English, German - DIN
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DIN EN 14136:2004-08
Use of external quality assessment schemes in the assessment of the performance of in vitro diagnostic examination procedures; German version EN 14136:2004
8/1/2004 - PDF - German - DIN
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DIN EN 14136:2004-08
Use of external quality assessment schemes in the assessment of the performance of in vitro diagnostic examination procedures; German version EN 14136:2004
8/1/2004 - PDF - English - DIN
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€79.72
-
DIN EN 13975:2003-11
Sampling procedures used for acceptance testing of in vitro diagnostic medical devices - Statistical aspects; German version EN 13975:2003, German and English texts
11/1/2003 - PDF - English, German - DIN
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DIN EN ISO 18153:2003-11
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); German version EN ISO 18153:2003
11/1/2003 - PDF - German - DIN
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DIN EN ISO 18153:2003-11
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); German version EN ISO 18153:2003
11/1/2003 - PDF - English - DIN
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DIN 58932-4:2003-07
Haematology - Determination of the concentration of blood corpuscles in blood - Part 4: Reference procedure for the determination of the concentration of leucocytes
7/1/2003 - PDF - English, German - DIN
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DIN EN 13612:2002-08
Performance evaluation of in vitro diagnostic medical devices; German version EN 13612:2002, German and English texts
8/1/2002 - PDF - English, German - DIN
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DIN EN 13641:2002-08
Elimination or reduction of risk of infection related to in vitro diagnostic reagents; German version EN 13641:2002, German and English texts
8/1/2002 - PDF - English, German - DIN
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DIN EN 13532:2002-08
General requirements for in vitro diagnostic medical devices for self-testing; German version EN 13532:2002, German and English texts
8/1/2002 - PDF - English, German - DIN
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DIN 58930:2002-08
Haemostaseology - INR calibration plasmas - Requirements, preparation and use
8/1/2002 - PDF - English, German - DIN
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DIN 12847-2:2000-05
Laboratory glassware - Haemacytometer counting chambers - Rulings
5/1/2000 - PDF - German - DIN
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DIN 58901-1:2000-03
Haemostaseology - Determination of factor VII coagulant activity (F VII C) - Part 1: Reference measurement procedure for the one-stage method
3/1/2000 - PDF - English, German - DIN
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DIN 58901-2:2000-03
Haemostaseology - Determination of factor VII coagulant activity (F VII C) - Part 2: Reference measurement procedure using a synthetic peptide substrate
3/1/2000 - PDF - English, German - DIN
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DIN 58906-1:2000-03
Haemostaseology - Determination of fibrinogen concentration - Part 1: Reference measurement procedure for the determination of clottable fibrinogen as described by Clauss
3/1/2000 - PDF - English, German - DIN
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DIN 58907-1:2000-03
Haemostaseology - Determination of factor IX coagulant activity (F IX C) - Part 1: Reference measurement procedure for the one-stage method
3/1/2000 - PDF - English, German - DIN
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DIN 58910-2:2000-03
Haemostaseology - Determination of thromboplastin (prothrombin) time - Part 2: Reference measurement procedure for the determination in citrated venous blood
3/1/2000 - PDF - English, German - DIN
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DIN 58910-3:2000-03
Haemostaseology - Determination of the thromboplastin (prothrombin) time - Part 3: Reference measurement procedure for the determination in citrated capillary blood
3/1/2000 - PDF - English, German - DIN
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DIN 58910-4:2000-03
Haemostaseology - Determination of thromboplastin (prothrombin) time - Part 4: Reference measurement procedure for the determination in capillary blood
3/1/2000 - PDF - English, German - DIN
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DIN 58911-1:2000-03
Haemostaseology - Calibration of measurement procedures - Part 1: Clotting time measurement procedures
3/1/2000 - PDF - English, German - DIN
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DIN 58911-2:2000-03
Haemostaseology - Calibration of measurement procedures - Part 2: Photometric measurement procedures
3/1/2000 - PDF - English, German - DIN
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DIN 58913-1:2000-03
Haemostaseology - Determination of factor II coagulant activity (F II C) and factor X coagulant activity (F X C) - Part 1: Reference measurement procedure for the one-stage method
3/1/2000 - PDF - English, German - DIN
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DIN 58914-1:2000-03
Haemostaseology - Determination of thrombin time - Part 1: Reference measurement procedure for the determination in plasma from citrated venous blood
3/1/2000 - PDF - English, German - DIN
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DIN 58939-1:2000-03
Haemostaseology - Reference plasma - Part 1: Requirements, preparation
3/1/2000 - PDF - English, German - DIN
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DIN 58932-2:1998-06
Haematology - Determination of the concentration of blood corpuscles in blood - Part 2: Characteristic quantities for erythrocytes (erythrocyte indices)
6/1/1998 - PDF - German - DIN
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DIN 58932-2:1998-06
Haematology - Determination of the concentration of blood corpuscles in blood - Part 2: Characteristic quantities for erythrocytes (erythrocyte indices)
6/1/1998 - PDF - English - DIN
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DIN 58904:1998-04
Haemostaseology - Determination of protein C activity - Reference measurement procedure with a chromogenic peptide substrate
4/1/1998 - PDF - English, German - DIN
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DIN 58934-1:1997-12
Haematology - Control material for the CBC - Part 1: Control bloods
12/1/1997 - PDF - German - DIN
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DIN 58935-1:1997-12
Hämatologie - Determination of the erythrocyte sedimentation rate in blood - Part 1: Selected method
12/1/1997 - PDF - German - DIN
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DIN 58933-1:1995-01
Haematology - Procedure for determining the volume fraction of erythrocytes (packed cell volume) in blood - Part 1: Reference method based on centrifugation
1/1/1995 - PDF - German - DIN
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DIN 12847-1:1984-05
Laboratory glassware; haemacytometer counting chambers; general requirements
5/1/1984 - PDF - German - DIN
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€22.99