11.100 : Laboratory medicine
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UNE-EN ISO 10993-14:2009
Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001)
9/9/2009 - PDF - English - AENOR
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UNE-EN ISO 10993-17:2009
Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)
9/9/2009 - PDF - Spanish - AENOR
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UNE-EN ISO 10993-17:2009
Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)
9/9/2009 - PDF - English - AENOR
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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
Learn More€99.44 -
NF EN ISO 10993-14, S99-501-14 (08/2009)
Biological evaluation of medical devices - Part 14 : identification and quantification of degradation products from ceramics
8/1/2009 - Paper - French - AFNOR
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BS EN ISO 10993-5:2009
Biological evaluation of medical devices Tests for in vitro cytotoxicity
7/31/2009 - PDF - English - BSI
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NBN EN ISO 15193:2009
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)
7/17/2009 - PDF - French - NBN
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NBN EN ISO 15193:2009
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)
7/17/2009 - PDF - German - NBN
Learn More€121.00 -
NBN EN ISO 15193:2009
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)
7/17/2009 - PDF - English - NBN
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NBN 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 (ISO 15194:2009)
7/17/2009 - PDF - French - NBN
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NBN 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 (ISO 15194:2009)
7/17/2009 - PDF - German - NBN
Learn More€89.00 -
NBN 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 (ISO 15194:2009)
7/17/2009 - PDF - English - NBN
Learn More€89.00 -
NBN EN ISO 10993-14:2009
Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001)
7/17/2009 - PDF - French - NBN
Learn More€58.00 -
NBN EN ISO 10993-14:2009
Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001)
7/17/2009 - PDF - German - NBN
Learn More€58.00 -
NBN EN ISO 10993-14:2009
Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001)
7/17/2009 - PDF - English - NBN
Learn More€58.00 -
BS EN ISO 10993-14:2009
Biological evaluation of medical devices Identification and quantification degradation products from ceramics
6/30/2009 - PDF - English - BSI
Learn More€180.00 -
UNE-EN ISO 10993-7:2009
Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2008)
6/3/2009 - PDF - Spanish - AENOR
Learn More€130.00 -
UNE-EN ISO 10993-7:2009
Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2008)
6/3/2009 - PDF - English - AENOR
Learn More€156.00 -
ISO 10993-5:2009 (R2017)
Biological evaluation of medical devices
Part 5: Tests for in vitro cytotoxicity
5/20/2009 - Paper - French - ISO
Learn More€174.00 -
ISO 15193:2009 (R2015)
In vitro diagnostic medical devices
Measurement of quantities in samples of biological origin
4/28/2009 - Paper - French - ISO
Learn More€148.00 -
ISO 15194:2009 (R2015)
In vitro diagnostic medical devices
Measurement of quantities in samples of biological origin
4/28/2009 - Paper - French - ISO
Learn More€110.00 -
€62.66 -
ASTM F2721-09(2023)
Standard Guide for Preclinicalin vivo Evaluation in Critical-Size Segmental Bone Defects
1/1/2009 - PDF - English - ASTM
Learn More€60.00 -
ASTM F2721-09(2023) + Redline
Standard Guide for Preclinicalin vivo Evaluation in Critical-Size Segmental Bone Defects
1/1/2009 - PDF - English - ASTM
Learn More€72.00 -
ASTM F639-09(2015)
Standard Specification for Polyethylene Plastics for Medical Applications
1/1/2009 - PDF - English - ASTM
Learn More€46.00 -
ASTM F639-09(2015) + Redline
Standard Specification for Polyethylene Plastics for Medical Applications
1/1/2009 - PDF - English - ASTM
Learn More€53.00 -
ASTM F624-09(2015)e1
Standard Guide for Evaluation of Thermoplastic Polyurethane Solids and Solutions for Biomedical Applications
1/1/2009 - PDF - English - ASTM
Learn More€46.00 -
ASTM F624-09(2015)e1 + Redline
Standard Guide for Evaluation of Thermoplastic Polyurethane Solids and Solutions for Biomedical Applications
1/1/2009 - PDF - English - ASTM
Learn More€53.00 -
NBN EN ISO 10993-7:2008
Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2008)
12/17/2008 - PDF - French - NBN
Learn More€208.00 -
NBN EN ISO 10993-7:2008
Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2008)
12/17/2008 - PDF - German - NBN
Learn More€208.00 -
NBN EN ISO 10993-7:2008
Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2008) + AC:2009
12/17/2008 - PDF - English - NBN
Learn More€208.00 -
NF EN ISO 10993-7, S99-501-7 (12/2008)
Biological evaluation of medical devices - Part 7 : ethylene oxide sterilization residuals
12/1/2008 - Paper - French - AFNOR
Learn More€167.00 -
ISO 24998:2008 (R2022)
Plastics laboratory ware
Single-use Petri dishes for microbiological procedures
11/14/2008 - Paper - French - ISO
Learn More€72.00 -
ISO 10993-7:2008 (R2016)
Biological evaluation of medical devices
Part 7: Ethylene oxide sterilization residuals
10/13/2008 - Paper - French - ISO
Learn More€248.00 -
UNE-EN ISO 22442-3:2008
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)
6/25/2008 - PDF - Spanish - AENOR
Learn More€74.00 -
UNE-EN ISO 22442-3:2008
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)
6/25/2008 - PDF - English - AENOR
Learn More€88.80 -
NBN EN ISO 22442-3:2008
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)
3/20/2008 - PDF - French - NBN
Learn More€121.00 -
NBN EN ISO 22442-3:2008
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)
3/20/2008 - PDF - German - NBN
Learn More€121.00 -
NBN EN ISO 22442-3:2008
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)
3/20/2008 - PDF - English - NBN
Learn More€121.00 -
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
Learn More€92.62 -
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
Learn More€115.98 -
BS EN ISO 22442-3:2007
Medical devices utilizing animal tissues and their derivatives Validation of the elimination and/or inactivation viruses transmissible spongiform encephalopathy (TSE) agents
2/29/2008 - PDF - English - BSI
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UNE-EN ISO 20776-2:2008
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 (ISO 20776-2:2007)
1/16/2008 - PDF - Spanish - AENOR
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UNE-EN ISO 20776-2:2008
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 (ISO 20776-2:2007)
1/16/2008 - PDF - English - AENOR
Learn More€72.00 -
ISO 22442-3:2007 (R2022)
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
11/27/2007 - Paper - French - ISO
Learn More€148.00 -
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
Learn More€104.95 -
DD ISO/TS 10993-20:2006
Biological evaluation of medical devices Principles and methods for immunotoxicology testing
9/29/2006 - PDF - English - BSI
Learn More€250.00 -
UNE-EN 14254:2004 (R2019)
In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humans
12/24/2004 - PDF - Spanish - AENOR
Learn More€68.00 -
UNE-EN 14254:2004 (R2019)
In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humans
12/24/2004 - PDF - English - AENOR
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UNE-EN 14136:2004 (R2020)
Use of external quality assessment schemes in the assessment of the performance of in vitro diagnostic examination procedures
12/10/2004 - PDF - Spanish - AENOR
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UNE-EN 14136:2004 (R2020)
Use of external quality assessment schemes in the assessment of the performance of in vitro diagnostic examination procedures
12/10/2004 - PDF - English - AENOR
Learn More€72.00 -
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
Learn More€82.52 -
BS ISO 15198:2004
Clinical laboratory medicine. In vitro diagnostic medical devices. Validation of user quality control procedures by the manufacturer
7/23/2004 - PDF - English - BSI
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NBN EN 14136:2004
Use of external quality assessment schemes in the assessment of the performance of in vitro diagnostic examination procedures
6/30/2004 - PDF - French - NBN
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NBN EN 14136:2004
Use of external quality assessment schemes in the assessment of the performance of in vitro diagnostic examination procedures
6/30/2004 - PDF - German - NBN
Learn More€58.00 -
NBN EN 14136:2004
Use of external quality assessment schemes in the assessment of the performance of in vitro diagnostic examination procedures
6/30/2004 - PDF - English - NBN
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BS EN 14136:2004
Use of external quality assessment schemes in the assessment of the performance of in vitro diagnostic examination procedures
5/26/2004 - PDF - English - BSI
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UNE-EN 13975:2003 (R2020)
Sampling procedures used for acceptance testing of in vitro diagnostic medical devices - Statistical aspects
12/12/2003 - PDF - Spanish - AENOR
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UNE-EN 13975:2003 (R2020)
Sampling procedures used for acceptance testing of in vitro diagnostic medical devices - Statistical aspects
12/12/2003 - PDF - English - AENOR
Learn More€72.00 -
€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
Learn More€79.72 -
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
Learn More€72.80 -
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
Learn More€91.12 -
BS 3985:2003
Haemiglobincyanide (cyanmethaemoglobin) preparation as a standard for spectrometric haemoglobinometry
10/10/2003 - PDF - English - BSI
Learn More€151.00 -
NBN EN ISO 18153:2003
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)
9/30/2003 - PDF - French - NBN
Learn More€58.00 -
NBN EN ISO 18153:2003
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)
9/30/2003 - PDF - German - NBN
Learn More€58.00 -
NBN EN ISO 18153:2003
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)
9/30/2003 - PDF - English - NBN
Learn More€58.00 -
BS EN ISO 18153:2003
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
8/19/2003 - PDF - English - BSI
Learn More€180.00 -
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
Learn More€85.79 -
BS EN ISO 18812:2003
Health informatics. Clinical analyser interfaces to laboratory information systems. Use profiles
6/24/2003 - PDF - English - BSI
Learn More€348.00 -
NBN EN 13975:2003
Sampling procedures used for acceptance testing of in vitro diagnostic medical devices - Statistical aspects
4/25/2003 - PDF - French - NBN
Learn More€58.00 -
NBN EN 13975:2003
Sampling procedures used for acceptance testing of in vitro diagnostic medical devices - Statistical aspects
4/25/2003 - PDF - German - NBN
Learn More€58.00 -
NBN EN 13975:2003
Sampling procedures used for acceptance testing of in vitro diagnostic medical devices - Statistical aspects
4/25/2003 - PDF - English - NBN
Learn More€58.00 -
BS EN 13975:2003
Sampling procedures used for acceptance testing of in vitro diagnostic medical devices. Statistical aspects
3/28/2003 - PDF - English - BSI
Learn More€180.00 -
UNE-EN 13612/AC:2003 (R2014)
Performance evaluation of in vitro diagnostic medical devices.
3/21/2003 - PDF - Spanish - AENOR
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UNE-EN 13612/AC:2003 (R2014)
Performance evaluation of in vitro diagnostic medical devices.
3/21/2003 - PDF - English - AENOR
Learn More€0.00 -
BS EN 13612:2002
Performance evaluation of in vitro diagnostic medical devices
2/27/2003 - PDF - English - BSI
Learn More€180.00 -
UNE-EN 13532:2002 (R2020)
General requirements for in vitro diagnostic medical devices for self-testing.
10/29/2002 - PDF - Spanish - AENOR
Learn More€49.00 -
UNE-EN 13532:2002 (R2020)
General requirements for in vitro diagnostic medical devices for self-testing.
10/29/2002 - PDF - English - AENOR
Learn More€58.80 -
UNE-EN 13641:2002 (R2020)
Elimination or reduction of risk of infection related to in vitro diagnostic reagents.
10/29/2002 - PDF - Spanish - AENOR
Learn More€49.00 -
UNE-EN 13641:2002 (R2020)
Elimination or reduction of risk of infection related to in vitro diagnostic reagents.
10/29/2002 - PDF - English - AENOR
Learn More€58.80 -
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
Learn More€72.80 -
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
Learn More€59.63 -
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
Learn More€59.63 -
DIN 58930:2002-08
Haemostaseology - INR calibration plasmas - Requirements, preparation and use
8/1/2002 - PDF - English, German - DIN
Learn More€39.35 -
UNE-EN 13612:2002 (R2020)
Performance evaluation of in vitro diagnostic medical devices.
7/29/2002 - PDF - Spanish - AENOR
Learn More€60.00 -
UNE-EN 13612:2002 (R2020)
Performance evaluation of in vitro diagnostic medical devices.
7/29/2002 - PDF - English - AENOR
Learn More€72.00 -
NBN EN 13641:2002
Elimination or reduction of risk of infection related to in vitro diagnostic reagents
7/17/2002 - PDF - French - NBN
Learn More€58.00 -
NBN EN 13641:2002
Elimination or reduction of risk of infection related to in vitro diagnostic reagents
7/17/2002 - PDF - German - NBN
Learn More€58.00 -
NBN EN 13641:2002
Elimination or reduction of risk of infection related to in vitro diagnostic reagents
7/17/2002 - PDF - English - NBN
Learn More€58.00 -
NBN EN 13532:2002
General requirements for in vitro diagnostic medical devices for self-testing
6/28/2002 - PDF - French - NBN
Learn More€58.00 -
NBN EN 13532:2002
General requirements for in vitro diagnostic medical devices for self-testing
6/28/2002 - PDF - German - NBN
Learn More€58.00 -
NBN EN 13532:2002
General requirements for in vitro diagnostic medical devices for self-testing
6/28/2002 - PDF - English - NBN
Learn More€58.00 -
BS EN 13641:2002
Elimination or reduction of risk of infection related to in vitro diagnostic reagents
5/27/2002 - PDF - English - BSI
Learn More€151.00 -
BS EN 13532:2002
General requirements for in vitro diagnostic medical devices for self-testing
5/8/2002 - PDF - English - BSI
Learn More€151.00 -
NBN EN 13612:2002
Performance evaluation of in vitro diagnostic medical devices
5/3/2002 - PDF - French - NBN
Learn More€89.00 -
NBN EN 13612:2002
Performance evaluation of in vitro diagnostic medical devices
5/3/2002 - PDF - German - NBN
Learn More€89.00 -
NBN EN 13612:2002
Performance evaluation of in vitro diagnostic medical devices
5/3/2002 - PDF - English - NBN
Learn More€89.00 -
ISO 10993-14:2001 (R2019)
Biological evaluation of medical devices
Part 14: Identification and quantification of degradation products from ceramics
11/22/2001 - Paper - French - ISO
Learn More€72.00 -
ASTM F2147-01(2016)
Standard Practice for Guinea Pig: Split Adjuvant and Closed Patch Testing for Contact Allergens
1/1/2001 - PDF - English - ASTM
Learn More€51.00 -
ASTM F2147-01(2016) + Redline
Standard Practice for Guinea Pig: Split Adjuvant and Closed Patch Testing for Contact Allergens
1/1/2001 - PDF - English - ASTM
Learn More€61.00 -
UNE 129002:2000 IN
Glossary of recommended terms in clinical laboratory sciences.
10/27/2000 - PDF - Spanish - AENOR
Learn More€110.00 -
DIN 12847-2:2000-05
Laboratory glassware - Haemacytometer counting chambers - Rulings
5/1/2000 - PDF - German - DIN
Learn More€32.34 -
UNE 129003:2000 EX
Nomenclature, syntax and expression of the values of biological quantities.
3/31/2000 - PDF - Spanish - AENOR
Learn More€90.00 -
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
Learn More€39.35 -
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
Learn More€39.35 -
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
Learn More€45.98 -
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
Learn More€39.35 -
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
Learn More€39.35 -
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
Learn More€39.35 -
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
Learn More€39.35 -
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
Learn More€45.98 -
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
Learn More€52.90 -
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
Learn More€39.35 -
DIN 58939-1:2000-03
Haemostaseology - Reference plasma - Part 1: Requirements, preparation
3/1/2000 - PDF - English, German - DIN
Learn More€45.98 -
€46.00 -
€53.00
-
ASTM F1984-99(2018)
Standard Practice for Testing for Whole Complement Activation in Serum by Solid Materials
1/1/1999 - PDF - English - ASTM
Learn More€51.00 -
ASTM F1984-99(2018) + Redline
Standard Practice for Testing for Whole Complement Activation in Serum by Solid Materials
1/1/1999 - PDF - English - ASTM
Learn More€61.00 -
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
Learn More€39.35 -
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
Learn More€49.16 -
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
Learn More€39.35 -
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
Learn More€39.35 -
NF S91-141 (11/1997) (R2012)
biodegradability of dental metal alloys. Standardization of electrochemical tests. - Biodégradabilité des alliages métalliques utilisés en art dentaire
11/1/1997 - Paper - French - AFNOR
Learn More€86.67 -
BS ISO 12771:1997
Plastics laboratory ware. Disposable serological pipettes
9/15/1997 - PDF - English - BSI
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BS ISO 12772:1997
Laboratory glassware. Disposable microhaematocrit capillary tubes
8/15/1997 - PDF - English - BSI
Learn More€151.00 -
€49.00
-
ASTM E961-97(2021)
Standard Specification for Blood Sedimentation Tube, Wintrobe, Glass, Reusable
1/1/1997 - PDF - English - ASTM
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ASTM E961-97(2021) + Redline
Standard Specification for Blood Sedimentation Tube, Wintrobe, Glass, Reusable
1/1/1997 - PDF - English - ASTM
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ASTM E923-97(2019)
Standard Specification for Glass Westergren Tube, Reusable
1/1/1997 - PDF - English - ASTM
Learn More€46.00 -
ASTM E923-97(2019) + Redline
Standard Specification for Glass Westergren Tube, Reusable
1/1/1997 - PDF - English - ASTM
Learn More€53.00 -
€46.00 -
€53.00
-
ASTM E1044-96(2024)
Standard Specification for Glass Serological Pipets (General Purpose and Kahn)
1/1/1996 - PDF - English - ASTM
Learn More€52.00 -
ASTM E1044-96(2024) + Redline
Standard Specification for Glass Serological Pipets (General Purpose and Kahn)
1/1/1996 - PDF - English - ASTM
Learn More€63.00 -
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
Learn More€39.35 -
ASTM E714-94(2021)
Standard Specification for Disposable Glass Serological Pipets
1/1/1994 - PDF - English - ASTM
Learn More€46.00 -
ASTM E714-94(2021) + Redline
Standard Specification for Disposable Glass Serological Pipets
1/1/1994 - PDF - English - ASTM
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ASTM E890-94(2021)
Standard Specification for Disposable Glass Culture Tubes
1/1/1994 - PDF - English - ASTM
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ASTM E890-94(2021) + Redline
Standard Specification for Disposable Glass Culture Tubes
1/1/1994 - PDF - English - ASTM
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ASTM E934-94(2021)
Standard Specification for Serological Pipet, Disposable Plastic
1/1/1994 - PDF - English - ASTM
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ASTM E934-94(2021) + Redline
Standard Specification for Serological Pipet, Disposable Plastic
1/1/1994 - PDF - English - ASTM
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ASTM E1093-91(2019)
Standard Specification for Glass Prothrombin Pipet, Disposable
1/1/1991 - PDF - English - ASTM
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ASTM E1093-91(2019) + Redline
Standard Specification for Glass Prothrombin Pipet, Disposable
1/1/1991 - PDF - English - ASTM
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ASTM E1092-91(2022)
Standard Specification for Glass Micro Folin Pipet, Disposable
1/1/1991 - PDF - English - ASTM
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ASTM E1092-91(2022) + Redline
Standard Specification for Glass Micro Folin Pipet, Disposable
1/1/1991 - PDF - English - ASTM
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ASTM E1380-90(2021)
Standard Specification for Color Coding of Laboratory Pipets with Multiple Graduations, 0.1 mL and Larger, But Excluding Disposable Prothrombin and Disposable Micropipets
1/1/1990 - PDF - English - ASTM
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ASTM E1380-90(2021) + Redline
Standard Specification for Color Coding of Laboratory Pipets with Multiple Graduations, 0.1 mL and Larger, But Excluding Disposable Prothrombin and Disposable Micropipets
1/1/1990 - PDF - English - ASTM
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ASTM E1048-88(2021)
Standard Specification for Color-Coding Pipets or Containers Coated With Anticoagulants
1/1/1988 - PDF - English - ASTM
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ASTM E1048-88(2021) + Redline
Standard Specification for Color-Coding Pipets or Containers Coated With Anticoagulants
1/1/1988 - PDF - English - ASTM
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€48.00
-
ASTM E1047-85(2021)
Standard Specification for Blood Sedimentation Tube, Wintrobe, Glass, Disposable
1/1/1985 - PDF - English - ASTM
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ASTM E1047-85(2021) + Redline
Standard Specification for Blood Sedimentation Tube, Wintrobe, Glass, Disposable
1/1/1985 - PDF - English - ASTM
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ASTM E1046-85(2021)
Standard Specification for Glass Westergren Tube, Disposable
1/1/1985 - PDF - English - ASTM
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ASTM E1046-85(2021) + Redline
Standard Specification for Glass Westergren Tube, Disposable
1/1/1985 - PDF - English - ASTM
Learn More€53.00 -
DIN 12847-1:1984-05
Laboratory glassware; haemacytometer counting chambers; general requirements
5/1/1984 - PDF - German - DIN
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ASTM E787-81(2024)
Standard Specification for Disposable Glass Micro Blood Collection Pipets
1/1/1981 - PDF - English - ASTM
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ASTM E787-81(2024) + Redline
Standard Specification for Disposable Glass Micro Blood Collection Pipets
1/1/1981 - PDF - English - ASTM
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ASTM E734-80(2021)
Standard Specification for Disposable Glass Blood Sample Capillary Tube (Microhematocrit)
1/1/1980 - PDF - English - ASTM
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ASTM E734-80(2021) + Redline
Standard Specification for Disposable Glass Blood Sample Capillary Tube (Microhematocrit)
1/1/1980 - PDF - English - ASTM
Learn More€53.00 -
€52.00 -
€63.00
-
€22.99
-
UNE-CEN/TS 17981-1:2023
In vitro diagnostic Next Generation Sequencing (NGS) workflows - Part 1: Human DNA examination (Endorsed by Asociación Española de Normalización in January of 2024.)
4/18/2024 - PDF - English - AENOR
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UNE-CEN/TS 17981-2:2023
In vitro diagnostic Next Generation Sequencing (NGS) workflows - Part 2: Human RNA examination (Endorsed by Asociación Española de Normalización in January of 2024.)
4/18/2024 - PDF - English - AENOR
Learn More€100.00
