11.100 : Laboratory medicine
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ASTM F756-17
Standard Practice for Assessment of Hemolytic Properties of Materials
3/1/2017 - PDF - English -
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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 -
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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 -
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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 -
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 -
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PD ISO/TR 15499:2016
Biological evaluation of medical devices. Guidance on the conduct of biological evaluation within a risk management process
1/31/2017 - PDF - English -
Learn More€250.00 -
NBN EN ISO 10993-6:2017
Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2016)
1/27/2017 - PDF - French -
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NBN EN ISO 10993-6:2017
Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2016)
1/27/2017 - PDF - German -
Learn More€142.00 -
NBN EN ISO 10993-6:2017
Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2016)
1/27/2017 - PDF - English -
Learn More€142.00 -
BS EN ISO 10993-6:2016
Biological evaluation of medical devices Tests for local effects after implantation
12/31/2016 - PDF - English -
Learn More€331.00 -
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 -
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PD ISO/TS 16782:2016
Clinical laboratory testing. Criteria for acceptable lots of dehydrated Mueller-Hinton agar and broth for antimicrobial susceptibility testing
11/30/2016 - PDF - English -
Learn More€250.00 -
ISO 10993-6:2016
Biological evaluation of medical devices
Part 6: Tests for local effects after implantation
11/28/2016 - Paper - French -
Learn More€174.00 -
ASTM F3142-16 + Redline
Standard Guide for Evaluation ofin vitro Release of Biomolecules from Biomaterials Scaffolds for TEMPs
11/15/2016 - PDF - English -
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ASTM F3142-16
Standard Guide for Evaluation ofin vitro Release of Biomolecules from Biomaterials Scaffolds for TEMPs
11/15/2016 - PDF - English -
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JIS T 6001/AMENDMENT 1:2016
Evaluation of biocompatibility of medical devices used in dentistry (Amendment 1)
10/1/2016 - PDF - Japanese -
Learn More€25.00 -
ASTM F3209-16
Standard Guide for Autologous Platelet-Rich Plasma for Use in Tissue Engineering and Cell Therapy
10/1/2016 - PDF - English -
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ASTM F3209-16 + Redline
Standard Guide for Autologous Platelet-Rich Plasma for Use in Tissue Engineering and Cell Therapy
10/1/2016 - PDF - English -
Learn More€61.00 -
ASTM E2548-16 + Redline
Standard Guide for Sampling Seized Drugs for Qualitative and Quantitative Analysis
3/1/2016 - PDF - English -
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ASTM E2548-16
Standard Guide for Sampling Seized Drugs for Qualitative and Quantitative Analysis
3/1/2016 - PDF - English -
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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 -
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BS 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
1/31/2016 - PDF - English -
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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
1/31/2016 - PDF - English -
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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 -
Learn More€136.82 -
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 -
Learn More€65.89 -
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 -
Learn More€170.93 -
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 -
Learn More€82.52 -
UNE-EN ISO 15197:2015
In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2013)
9/23/2015 - PDF - Spanish -
Learn More€100.00 -
UNE-EN ISO 23640:2015
In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)
9/23/2015 - PDF - English -
Learn More€69.60 -
UNE-EN ISO 15197:2015
In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2013)
9/23/2015 - PDF - English -
Learn More€120.00 -
UNE-EN ISO 23640:2015
In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)
9/23/2015 - PDF - Spanish -
Learn More€58.00 -
DIN 58964:2015-09
Quality assurance of POCT results - Assessment criteria for comparison measurement and implementation
9/1/2015 - PDF - English -
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 -
Learn More€45.98 -
DIN 58964:2015-09
Quality assurance of POCT results - Assessment criteria for comparison measurement and implementation
9/1/2015 - PDF - German -
Learn More€65.89 -
XP ISO/TS 17518, S92-042 (09/2015)
Medical Laboratories - Reagents for staining biological material - Guidance for users
9/1/2015 - Paper - French -
Learn More€75.50 -
NBN EN ISO 15197:2015
In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2013)
7/24/2015 - PDF - French -
Learn More€163.00 -
NBN EN ISO 23640:2015
In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)
7/24/2015 - PDF - German -
Learn More€58.00 -
NBN EN ISO 15197:2015
In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2013)
7/24/2015 - PDF - German -
Learn More€163.00 -
NBN EN ISO 23640:2015
In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)
7/24/2015 - PDF - English -
Learn More€58.00 -
NBN EN ISO 23640:2015
In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)
7/24/2015 - PDF - French -
Learn More€58.00 -
NBN EN ISO 15197:2015
In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2013)
7/24/2015 - PDF - English -
Learn More€163.00 -
BS EN ISO 15197:2015
In vitro diagnostic test systems. Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus
6/30/2015 - PDF - English -
Learn More€348.00 -
BS EN ISO 23640:2015
In vitro diagnostic medical devices. Evaluation of stability of in vitro diagnostic reagents
6/30/2015 - PDF - English -
Learn More€180.00 -
ASTM E3002-15(2023) + Redline
Standard Practice for Assessing the Comparative Efficacy of Products Used for the Decontamination of Chemical Warfare Agents (CWAs) on Skin
6/15/2015 - PDF - English -
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ASTM E3002-15(2023)
Standard Practice for Assessing the Comparative Efficacy of Products Used for the Decontamination of Chemical Warfare Agents (CWAs) on Skin
6/15/2015 - PDF - English -
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PD ISO/TS 17518:2015
Medical laboratories. Reagents for staining biological material. Guidance for users
5/31/2015 - PDF - English -
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UNE-EN ISO 10993-3:2015
Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:2014)
5/6/2015 - PDF - English -
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UNE-EN ISO 10993-3:2015
Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:2014)
5/6/2015 - PDF - Spanish -
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NF EN 455-3, S97-001-3 (05/2015)
Medical gloves for single use - Part 3 : requirements and testing for biological evaluation
5/1/2015 - Paper - French -
Learn More€93.00 -
ISO/TS 17518:2015 (R2022)
Medical laboratories
Reagents for staining biological material
4/16/2015 - Paper - French -
Learn More€110.00 -
PD ISO/TR 10993-33:2015
Biological evaluation of medical devices Guidance on tests to evaluate genotoxicity. Supplement ISO 10993-3
3/31/2015 - PDF - English -
Learn More€348.00 -
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 -
Learn More€115.33 -
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 -
Learn More€144.02 -
PD ISO/TS 17822-1:2014
In vitro diagnostic test systems. Qualitative nucleic acid-based in examination procedures for detection and identification of microbial pathogens General requirements, terms definitions
12/31/2014 - PDF - English -
Learn More€293.00 -
NF EN ISO 10993-3, S99-501-3 (12/2014)
Biological evaluation of medical devices - Part 3 : tests for genotoxicity, carcinogenicity and reproductive toxicity
12/1/2014 - Paper - French -
Learn More€108.00 -
NBN EN ISO 10993-3:2014
Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:2014)
11/28/2014 - PDF - German -
Learn More€142.00 -
NBN EN ISO 10993-3:2014
Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:2014)
11/28/2014 - PDF - English -
Learn More€142.00 -
NBN EN ISO 10993-3:2014
Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:2014)
11/28/2014 - PDF - French -
Learn More€142.00 -
BS EN ISO 10993-3:2014
Biological evaluation of medical devices Tests for genotoxicity, carcinogenicity and reproductive toxicity
10/31/2014 - PDF - English -
Learn More€331.00 -
ISO 10993-3:2014 (R2023)
Biological evaluation of medical devices
Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity
9/24/2014 - Paper - French -
Learn More€174.00 -
14/30264453 DC:2014
BS ISO 16782. Clinical laboratory testing. Criteria for acceptable lots of dehydrated Mueller-Hinton agar and broth for antimicrobial susceptibility testing
6/26/2014 - PDF - English -
Learn More€24.00 -
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 -
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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 -
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UNE 179007:2013
Health services. Systems of quality management for assisted reproduction laboratories
11/27/2013 - PDF - English -
Learn More€106.80 -
UNE-EN ISO 19001:2013
In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology (ISO 19001:2013)
11/27/2013 - PDF - Spanish -
Learn More€68.00 -
UNE-EN ISO 19001:2013
In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology (ISO 19001:2013)
11/27/2013 - PDF - English -
Learn More€81.60 -
UNE 179007:2013
Health services. Systems of quality management for assisted reproduction laboratories
11/27/2013 - PDF - Spanish -
Learn More€89.00 -
ASTM F2211-13(2021)
Standard Classification for Tissue-Engineered Medical Products (TEMPs)
10/1/2013 - PDF - English -
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DIN EN 61326-2-6 VDE 0843-20-2-6:2013-09
Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment (IEC 61326-2-6:2012), German version EN 61326-2-6:2013
9/1/2013 - Paper - German -
Learn More€53.63 -
NF EN 61326-2-6, C46-050-2-6 (09/2013)
Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 2-6 : particular requirements - In vitro diagnostic (IVD) medical equipment - Matériel électrique de mesure, de commande et de laboratoire
9/1/2013 - Paper - French -
Learn More€88.33 -
BS EN ISO 19001:2013
In vitro diagnostic medical devices. Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology
8/31/2013 - PDF - English -
Learn More€250.00 -
UNE-EN ISO 16256:2013
Clinical laboratory testing and in vitro diagnostic test systems - Reference method for testing the in vitro activity of antimicrobial agents against yeast of fungi involved in infectious diseases (ISO 16256:2012)
7/24/2013 - PDF - Spanish -
Learn More€68.00 -
UNE-EN ISO 16256:2013
Clinical laboratory testing and in vitro diagnostic test systems - Reference method for testing the in vitro activity of antimicrobial agents against yeast of fungi involved in infectious diseases (ISO 16256:2012)
7/24/2013 - PDF - English -
Learn More€81.60 -
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 -
Learn More€99.44 -
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 -
Learn More€79.72 -
NBN EN ISO 19001:2013
In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology (ISO 19001:2013)
6/21/2013 - PDF - French -
Learn More€89.00 -
NBN EN ISO 19001:2013
In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology (ISO 19001:2013)
6/21/2013 - PDF - English -
Learn More€89.00 -
UNE-EN ISO 15189:2013
Medical laboratories - Requirements for quality and competence (ISO 15189:2012, Corrected version 2014-08-15)
6/12/2013 - PDF - Spanish -
Learn More€102.00 -
UNE-EN ISO 15189:2013
Medical laboratories - Requirements for quality and competence (ISO 15189:2012, Corrected version 2014-08-15)
6/12/2013 - PDF - English -
Learn More€122.40 -
ISO 15197:2013 (R2018)
In vitro diagnostic test systems
Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus
5/14/2013 - Paper - French -
Learn More€199.00 -
€85.98 -
€68.60
-
NF S92-503 (03/2013)
Laboratory of medical biology - Anthroporadiometric measurements - Thyroid - Measurement of gamma-ray emissions of isotopes of iodine - Laboratoire d'analyses de biologie médicale
3/1/2013 - Paper - French -
Learn More€75.67 -
NF S92-501 (03/2013)
Laboratory of medical biology - Anthroporadiometric measurements - Whole body - Measurement of gamma-ray emissions of energy greater than 100 keV - Laboratoire d'analyses de biologie médicale
3/1/2013 - Paper - French -
Learn More€60.67 -
NF S92-502 (03/2013)
Laboratory of medical biology - Anthroporadiometric measurements - Lungs - Measurement of X-ray and gamma-ray emissions of energy less than 200 keV - Laboratoire d'analyses de biologie médicale
3/1/2013 - Paper - French -
Learn More€60.67 -
ASTM D7225-13(2019)e1
Standard Guide for Blood Cleaning Efficiency of Detergents and Washer-Disinfectors
1/1/2013 - PDF - English -
Learn More€46.00 -
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 -
Learn More€72.80 -
ASTM F2529-13(2021) + Redline
Standard Guide for?in vivo Evaluation of Osteoinductive Potential for Materials Containing Demineralized Bone (DBM)
1/1/2013 - PDF - English -
Learn More€68.00 -
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 -
Learn More€164.95 -
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 -
Learn More€72.80 -
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 -
Learn More€91.12 -
ASTM D7225-13(2019)e1 + Redline
Standard Guide for Blood Cleaning Efficiency of Detergents and Washer-Disinfectors
1/1/2013 - PDF - English -
Learn More€53.00 -
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 -
Learn More€131.96 -
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 -
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), German version EN ISO 18113-4:2011.
1/1/2013 - PDF - German -
Learn More€72.80 -
ASTM F2529-13(2021)
Standard Guide for?in vivo Evaluation of Osteoinductive Potential for Materials Containing Demineralized Bone (DBM)
1/1/2013 - PDF - English -
Learn More€57.00 -
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 -
Learn More€91.12 -
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 -
Learn More€72.80 -
ASTM F2211-13(2021) + Redline
Standard Classification for Tissue-Engineered Medical Products (TEMPs)
1/1/2013 - PDF - English -
Learn More€61.00 -
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 -
Learn More€91.12 -
NF EN ISO 15189, S92-060 (12/2012)
Medical laboratories - Requirements for quality and competence - Laboratoires d'analyses de biologie médicale
12/1/2012 - Paper - French -
Learn More€59.33 -
JIS Z 2801:2010/AMENDMENT 1:2012 (R2017)
Antibacterial products -- Test for antibacterial activity and efficacy (Amendment 1)
5/21/2012 - PDF - English -
Learn More€13.00 -
NF EN ISO 18113-5, S92-010-5 (05/2012)
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5 : in vitro diagnostic instruments for self-testing - Dispositifs médicaux de diagnostic in vitro
5/1/2012 - Paper - French -
Learn More€58.33 -
NF EN ISO 18113-4, S92-010-4 (05/2012)
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4 : in vitro diagnostic reagents for self-testing - Dispositifs médicaux de diagnostic in vitro
5/1/2012 - Paper - French -
Learn More€70.75 -
JIS T 0993-1:2012 (R2016)
Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process
3/1/2012 - PDF - Japanese -
Learn More€36.27 -
JIS T 6001:2012
Evaluation of biocompatibility of medical devices used in dentistry
3/1/2012 - PDF - Japanese -
Learn More€41.86 -
JIS T 0993-7:2012 (R2016)
Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals
3/1/2012 - PDF - Japanese -
Learn More€58.50 -
UNE-EN ISO 18113-2:2012
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009)
2/22/2012 - PDF - Spanish -
Learn More€68.00 -
UNE-EN ISO 18113-4:2012
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009)
2/22/2012 - PDF - English -
Learn More€81.60 -
UNE-EN ISO 18113-1:2012
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)
2/22/2012 - PDF - Spanish -
Learn More€95.00 -
UNE-EN ISO 18113-3:2012
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009)
2/22/2012 - PDF - English -
Learn More€72.00 -
UNE-EN ISO 18113-2:2012
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009)
2/22/2012 - PDF - English -
Learn More€81.60 -
UNE-EN ISO 18113-5:2012
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009)
2/22/2012 - PDF - Spanish -
Learn More€60.00 -
UNE-EN ISO 18113-1:2012
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)
2/22/2012 - PDF - English -
Learn More€114.00 -
UNE-EN ISO 18113-4:2012
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009)
2/22/2012 - PDF - Spanish -
Learn More€68.00 -
UNE-EN ISO 18113-3:2012
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009)
2/22/2012 - PDF - Spanish -
Learn More€60.00 -
UNE-EN ISO 18113-5:2012
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009)
2/22/2012 - PDF - English -
Learn More€72.00 -
BS EN ISO 18113-4:2011
In vitro diagnostic medical Devices. Information supplied by the manufacturer (labelling) reagents for self-testing
1/31/2012 - PDF - English -
Learn More€250.00 -
BS EN ISO 18113-1:2011
In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling) Terms, definitions and general requirements
1/31/2012 - PDF - English -
Learn More€348.00 -
BS EN ISO 18113-5:2011
In vitro diagnostic medical Devices. Information supplied by the manufacturer (labelling) instruments for self-testing
1/31/2012 - PDF - English -
Learn More€180.00 -
BS EN ISO 18113-2:2011
In vitro diagnostic medical Devices. Information supplied by the manufacturer (labelling) reagents for professional use
1/31/2012 - PDF - English -
Learn More€250.00 -
NBN EN ISO 18113-3:2011
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009)
12/14/2011 - PDF - German -
Learn More€58.00 -
NBN EN ISO 18113-2:2011
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009)
12/14/2011 - PDF - French -
Learn More€58.00 -
NBN EN ISO 18113-1:2011
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)
12/14/2011 - PDF - German -
Learn More€58.00 -
NBN EN ISO 18113-5:2011
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009)
12/14/2011 - PDF - English -
Learn More€58.00 -
NBN EN ISO 18113-4:2011
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009)
12/14/2011 - PDF - German -
Learn More€58.00 -
NBN EN ISO 18113-5:2011
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009)
12/14/2011 - PDF - French -
Learn More€58.00 -
NBN EN ISO 18113-3:2011
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009)
12/14/2011 - PDF - English -
Learn More€58.00 -
NBN EN ISO 18113-2:2011
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009)
12/14/2011 - PDF - German -
Learn More€58.00 -
NBN EN ISO 18113-1:2011
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)
12/14/2011 - PDF - English -
Learn More€58.00 -
NBN EN ISO 18113-3:2011
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009)
12/14/2011 - PDF - French -
Learn More€58.00 -
NBN EN ISO 18113-4:2011
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009)
12/14/2011 - PDF - English -
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NBN EN ISO 18113-1:2011
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)
12/14/2011 - PDF - French -
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NBN EN ISO 18113-5:2011
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009)
12/14/2011 - PDF - German -
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NBN EN ISO 18113-4:2011
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009)
12/14/2011 - PDF - French -
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NBN EN ISO 18113-2:2011
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009)
12/14/2011 - PDF - English -
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BS EN ISO 18113-3:2011
In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling) instruments for professional use
11/30/2011 - PDF - English -
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ISO 23640:2011 (R2018)
In vitro diagnostic medical devices
Evaluation of stability of in vitro diagnostic reagents
11/29/2011 - Paper - French -
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€62.40 -
UNE-EN ISO 13079:2011
Laboratory glass and plastics ware. Tubes and support for the measurement of erythrocytic sedimentation rate by the Westergren method (ISO 13079:2011)
11/16/2011 - PDF - Spanish -
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€52.00
-
UNE-EN ISO 13079:2011
Laboratory glass and plastics ware. Tubes and support for the measurement of erythrocytic sedimentation rate by the Westergren method (ISO 13079:2011)
11/16/2011 - PDF - English -
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NBN EN ISO 13079:2011
Laboratory glass and plastics ware - Tubes for the measurement of the erythrocyte sedimentation rate by the Westergren method (ISO 13079:2011)
9/23/2011 - PDF - English -
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€58.00
-
NBN EN ISO 13079:2011
Laboratory glass and plastics ware - Tubes for the measurement of the erythrocyte sedimentation rate by the Westergren method (ISO 13079:2011)
9/23/2011 - PDF - French -
Learn More€89.00 -
€58.00
-
NBN EN ISO 13079:2011
Laboratory glass and plastics ware - Tubes for the measurement of the erythrocyte sedimentation rate by the Westergren method (ISO 13079:2011)
9/23/2011 - PDF - German -
Learn More€89.00 -
€58.00
-
€151.00 -
BS EN ISO 13079:2011
Laboratory glass and plastics ware. Tubes for the measurement of the erythrocyte sedimentation rate by the Westergren method
8/31/2011 - PDF - English -
Learn More€250.00 -
€180.00 -
JIS T 3233:2011 (R2016)
Evacuated single-use containers for venous blood specimen collection
7/29/2011 - PDF - Japanese -
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€72.00
-
ISO 13079:2011 (R2023)
Laboratory glass and plastics ware
Tubes for the measurement of the erythrocyte sedimentation rate by the Westergren method
7/6/2011 - Paper - French -
Learn More€110.00 -
PD ISO/TR 22442-4:2010
Medical devices utilizing animal tissues and their derivatives Principles for elimination and/or inactivation of transmissible spongiform encephalopathy (TSE) agents validation assays those processes
2/28/2011 - PDF - English -
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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 -
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€61.00 -
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 -
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€51.00
-
UNE-EN ISO 10993-13:2010
Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:2010)
11/17/2010 - PDF - Spanish -
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UNE-EN ISO 10993-13:2010
Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:2010)
11/17/2010 - PDF - English -
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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 -
Learn More€107.48 -
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 -
Learn More€85.79 -
BS EN ISO 29701:2010
Nanotechnologies. Endotoxin test on nanomaterial samples for in vitro systems. Limulus amebocyte lysate (LAL) test
10/31/2010 - PDF - English -
Learn More€250.00 -
BS EN ISO 10993-13:2010
Biological evaluation of medical devices Identification and quantification degradation products from polymeric
10/31/2010 - PDF - English -
Learn More€250.00 -
NBN EN ISO 29701:2010
Nanotechnologies - Endotoxin test on nanomaterial samples for in vitro systems - Limulus amebocyte lysate (LAL) test (ISO 29701:2010)
10/29/2010 - PDF - English -
Learn More€121.00 -
NBN EN ISO 29701:2010
Nanotechnologies - Endotoxin test on nanomaterial samples for in vitro systems - Limulus amebocyte lysate (LAL) test (ISO 29701:2010)
10/29/2010 - PDF - French -
Learn More€121.00 -
NBN EN ISO 29701:2010
Nanotechnologies - Endotoxin test on nanomaterial samples for in vitro systems - Limulus amebocyte lysate (LAL) test (ISO 29701:2010)
10/29/2010 - PDF - German -
Learn More€121.00 -
UNE-EN ISO 29701:2010
Nanotechnologies - Endotoxin test on nanomaterial samples for in vitro systems - Limulus amebocyte lysate (LAL) test (ISO 29701:2010) (Endorsed by AENOR in October of 2010.)
10/1/2010 - PDF - English -
Learn More€68.00 -
ISO 29701:2010 (R2021)
Nanotechnologies
Endotoxin test on nanomaterial samples for in vitro systems
9/3/2010 - Paper - French -
Learn More€148.00 -
GB 19083-2010
Technical requirements for protective face mask for medical use
9/2/2010 - PDF - English -
Learn More€66.00 -
NF EN ISO 10993-13, S99-501-13 (09/2010)
Biological evaluation of medical devices - Part 13 : identification and quantification of degradation products from polymeric medical devices
9/1/2010 - Paper - French -
Learn More€75.50 -
NBN EN ISO 10993-13:2010
Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:2010)
7/30/2010 - PDF - French -
Learn More€89.00 -
NBN EN ISO 10993-13:2010
Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:2010)
7/30/2010 - PDF - German -
Learn More€89.00 -
NBN EN ISO 10993-13:2010
Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:2010)
7/30/2010 - PDF - English -
Learn More€89.00 -
NF EN ISO 10993-5, S99-501-5 (07/2010)
Biological evaluation of medical devices - Part 5 : tests for in vitro cytotoxicity
7/1/2010 - Paper - French -
Learn More€99.00 -
ISO 10993-13:2010 (R2019)
Biological evaluation of medical devices
Part 13: Identification and quantification of degradation products from polymeric medical devices
6/4/2010 - Paper - French -
Learn More€110.00 -
BS EN ISO 24998:2008
Plastics laboratory ware. Single-use Petri dishes for microbiological procedures
3/31/2010 - PDF - English -
Learn More€180.00 -
UNE-EN ISO 10993-7:2009/AC:2010
Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals - Technical Corrigendum 1 (ISO 10993-7:2008/Cor 1:2009)
2/24/2010 - PDF - Spanish -
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UNE-EN ISO 10993-7:2009/AC:2010
Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals - Technical Corrigendum 1 (ISO 10993-7:2008/Cor 1:2009)
2/24/2010 - PDF - English -
Learn More€0.00 -
UNE-EN ISO 10993-5:2009
Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009)
12/9/2009 - PDF - Spanish -
Learn More€85.00 -
UNE-EN ISO 10993-5:2009
Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009)
12/9/2009 - PDF - English -
Learn More€102.00 -
UNE-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)
11/25/2009 - PDF - Spanish -
Learn More€70.00 -
UNE-EN ISO 15194:2009 (R2014)
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)
11/25/2009 - PDF - Spanish -
Learn More€68.00 -
UNE-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)
11/25/2009 - PDF - English -
Learn More€84.00 -
UNE-EN ISO 15194:2009 (R2014)
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)
11/25/2009 - PDF - English -
Learn More€81.60 -
ISO 10993-7:2008/Cor 1:2009
Biological evaluation of medical devices
Part 7: Ethylene oxide sterilization residuals
11/12/2009 - Paper - French -
Learn More€0.00 -
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 -
Learn More€115.33 -
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 -
Learn More€92.62 -
NF EN ISO 15194, S92-020 (10/2009)
In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for certified reference materials and the content of supporting documentation - Dispositifs médicaux de diagnostic in vitro
10/1/2009 - Paper - French -
Learn More€75.67 -
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 -
Learn More€107.48 -
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 -
Learn More€144.02 -
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 -
Learn More€115.98 -
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 -
Learn More€85.79 -
NBN EN ISO 10993-5:2009
Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009)
9/11/2009 - PDF - French -
Learn More€142.00 -
NBN EN ISO 10993-5:2009
Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009)
9/11/2009 - PDF - German -
Learn More€142.00 -
NBN EN ISO 10993-5:2009
Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009)
9/11/2009 - PDF - English -
Learn More€142.00 -
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 -
Learn More€87.60 -
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 -
Learn More€81.60 -
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 -
Learn More€73.00
