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In vitro degradation reference

In vitro degradation reference, Total:81 items.

In the international standard classification, In vitro degradation reference involves: Medical equipment, Open systems interconnection (OSI), Character sets and information coding, Radiation protection, Radiation measurements, Animal feeding stuffs, Paint ingredients, Laboratory medicine, Medical sciences and health care facilities in general, Air quality.

Korean Agency for Technology and Standards (KATS), In vitro degradation reference

KS P 2093-2020 In-vitro degradation test of absorbable metals
KS P ISO 15814:2008 Implants for surgery－Copolymers and blends based on polylactide－In vitro degradation testing
KS P ISO 15814-2008(2013) Implants for surgery－Copolymers and blends based on polylactide－In vitro degradation testing
KS P ISO 13781:2019 Implants for surgery — Homopolymers, copolymers and blends on poly(lactide) — In vitro degradation testing
KS P ISO 16256:2017 Clinical laboratory testing and in vitro diagnostic test systems ─ Reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseases
KS P ISO 15193-2014(2019) In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Requirements for content and presentation of reference measurement procedures

American Society for Testing and Materials (ASTM), In vitro degradation reference

ASTM F1635-04 Standard Test Method for in Vitro Degradation Testing of Hydrolytically Degradable Polymer Resins and Fabricated Forms for Surgical Implants
ASTM F1635-11 Standard Test Method for in vitro Degradation Testing of Hydrolytically Degradable Polymer Resins and Fabricated Forms for Surgical Implants
ASTM F1635-04a Standard Test Method for in Vitro Degradation Testing of Hydrolytically Degradable Polymer Resins and Fabricated Forms for Surgical Implants
ASTM F1635-16 Standard Test Method for in vitro Degradation Testing of Hydrolytically Degradable Polymer Resins and Fabricated Forms for Surgical Implants
ASTM F1635-95 Standard Test Method for In Vitro Degradation Testing of Poly (L-lactic Acid) Resin and Fabricated Form for Surgical Implants
ASTM F1635-95(2000) Standard Test Method for In Vitro Degradation Testing of Poly (L-lactic Acid) Resin and Fabricated Form for Surgical Implants
ASTM D2621-87(2000) Standard Test Method for Infrared Identification of Vehicle Solids From Solvent-Reducible Paints
ASTM D2621-87(1995)e1 Standard Test Method for Infrared Identification of Vehicle Solids From Solvent-Reducible Paints
ASTM D2621-87(2016) Standard Test Method for Infrared Identification of Vehicle Solids From Solvent-Reducible Paints

国家药监局, In vitro degradation reference

YY/T 1806.1-2021 Evaluation method for in vitro degradation performance of biomedical materials Part 1: Degradable polyesters
YY/T 1806.2-2021 Methods for evaluation of in vitro degradation properties of biomedical materials Part 2: Mussel mucin
YY/T 1728-2021 Reference method for in vitro activity testing of yeast-like fungal antimicrobials related to systemic infectious diseases for clinical laboratory testing and in vitro diagnostics

Professional Standard - Medicine, In vitro degradation reference

YY/T 0473-2004 Implants for surgery-Copolymers and blends based on polylactide-In vitro degradation testing
YY/T 0474-2004 Poly(L-lactide) resins and fabricated forms for surgical implants-In vitro degradation testing

International Organization for Standardization (ISO), In vitro degradation reference

ISO 13781:1997 Poly(L-lactide) resins and fabricated forms for surgical implants - In vitro degradation testing
ISO/IEC 18384-2:2016 Information technology - Reference Architecture for Service Oriented Architecture (SOA RA) - Part 2: Reference Architecture for SOA Solutions
ISO 15814:1999 Implants for surgery - Copolymers and blends based on polylactide - In vitro degradation testing
ISO 13781:2017 Implants for surgery - Homopolymers, copolymers and blends on poly(lactide) - In vitro degradation testing
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

RU-GOST R, In vitro degradation reference

GOST R 59675-2021 Synthetic absorbable implantable surgical materials. In vitro degradation testing
GOST R ISO 15193-2015 In vitro medical devices. Measurement of quantities in samples of biological origin. Requirements for content and presentation of reference measurement procedures

British Standards Institution (BSI), In vitro degradation reference

BS IEC 61577-4:2009 Radiation protection instrumentation - Radon and radon decay product measuring instruments - Equipment for the production of reference atmospheres containing radon isotopes and their decay products (STAR)
BS ISO 13781:2017 Implants for surgery. Homopolymers, copolymers and blends on poly(lactide). In vitro degradation testing
BS EN 12286:1999(2001) In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Presentation of reference measurement procedures
BS EN 12286:1999 In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Presentation of reference measurement procedures
BS EN ISO 16256:2021 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
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

Canadian Standards Association (CSA), In vitro degradation reference

CAN/CSA-ISO/IEC 21000-8A:2010 Information technology - Multimedia framework (MPEG-21) - Part 8: Reference software - AMENDMENT 1: Extra reference software

American National Standards Institute （ANSI), In vitro degradation reference

ANSI/INCITS/ISO/IEC 21000-8/AMD 1:2011 Information technology - Multimedia framework (MPEG-21) - Part 8: Reference software; AMENDMENT 1: Extra reference software

International Electrotechnical Commission (IEC), In vitro degradation reference

IEC 61577-4:2009 Radiation protection instrumentation - Radon and radon decay product measuring instruments - Part 4: Equipment for the production of reference atmospheres containing radon isotopes and their decay products (STAR)

KR-KS, In vitro degradation reference

KS P ISO 13781-2019 Implants for surgery — Homopolymers, copolymers and blends on poly(lactide) — In vitro degradation testing
KS P ISO 16256-2017 Clinical laboratory testing and in vitro diagnostic test systems ─ Reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseases
KS P ISO 16256-2022 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 infec

Inner Mongolia Provincial Standard of the People's Republic of China, In vitro degradation reference

DB15/T 1164-2017 Determination of Degradation Rate of Neutral Detergent Fiber in Forage Grass Outside Rumen Fluid for 30 Hours
DB15/T 1165-2017 Determination of 7-hour Degradation Rate of Feed Corn and Silage Corn Starch in Rumen Fluid

CU-NC, In vitro degradation reference

NC 90-13-21-1984 Metrological Assurance. Spectrophotometers. Reference Dissolutions for the Verification of Spectrophotometers

PT-IPQ, In vitro degradation reference

NP EN 12286-2000 In vitro diagnostic medical devices Measurement of quantities in samples of boilogical origin Presentation of reference measurement procedures

European Committee for Standardization (CEN), In vitro degradation reference

EN ISO 16256:2021 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)
EN ISO 16256:2012 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)
CEN/TS 17405:2020 Stationary source emissions - Determination of the volume concentration of carbon dioxide - Reference method: infrared spectrometry
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)
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

Professional Standard - Hygiene , In vitro degradation reference

WS/T 253-2005 In vitro diagnostic medical devices Measurement of quantities in samples of biological origin Description of reference materials
WS/T 254-2005 In vitro diagnostic medical devices Measurement of quantities in samples of biological origin Presentation of reference measurement procedures

IT-UNI, In vitro degradation reference

UNI CEN/TS 17405-2020 Stationary source emissions - Determination of the volume concentration of carbon dioxide - Reference method: infrared spectrometry

Lithuanian Standards Office , In vitro degradation reference

LST CEN/TS 17405-2020 Stationary source emissions - Determination of the volume concentration of carbon dioxide - Reference method: infrared spectrometry

Association Francaise de Normalisation, In vitro degradation reference

XP CEN/TS 17405:2020 Emissions de sources fixes - Détermination de la concentration volumique en dioxyde de carbone - Méthode de référence : spectrométrie infrarouge
NF EN ISO 20776-1:2020 Sensibilité in vitro des agents infectieux et évaluation des performances des dispositifs pour antibiogrammes - Partie 1 : méthode de référence de microdilution en bouillon pour la détermination de la sensibilité in vitro aux agents antimicrobie...
NF EN ISO 16256:2021 Laboratoires d'analyses de biologie médicale et systèmes de diagnostic in vitro - Méthode de référence de microdilution en milieu liquide pour soumettre à essai l'activité in vitro des agents antimicrobiens par rapport aux levures impliquées ...
NF S92-012*NF EN ISO 16256:2021 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
NF EN ISO 15193:2009 Dispositifs médicaux de diagnostic in vitro - Mesurage des grandeurs dans des échantillons d'origine biologique - Exigences relatives au contenu et à la présentation des procédures de mesure de référence
NF EN ISO 15194:2009 Dispositifs médicaux de diagnostic in vitro - Mesurage des grandeurs dans les échantillons d'origine biologique - Exigences relatives aux matériaux de référence certifiés et au contenu de la documentation associée

German Institute for Standardization, In vitro degradation reference

DIN CEN/TS 17405:2020-11 Stationary source emissions - Determination of the volume concentration of carbon dioxide - Reference method: infrared spectrometry; German version CEN/TS 17405:2020
DIN CEN/TS 17405:2020 Stationary source emissions - Determination of the volume concentration of carbon dioxide - Reference method: infrared spectrometry; German version CEN/TS 17405:2020
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 I...
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
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
DIN EN ISO 16256:2021 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/DIS 16256:2021); German and English

General Administration of Quality Supervision, Inspection and Quarantine of the People‘s Republic of China, In vitro degradation reference

GB/T 19703-2005 In vitro diagnostic medical devices-Measurement of quantities in samples of biological origin-Description of reference materials
GB/T 19702-2005 In vitro diagnostic medical devices.Measurement of quantities in samples of biological origin.Presentation of reference measurement procedures

CEN - European Committee for Standardization, In vitro degradation reference

EN 12287:1999 In Vitro Diagnostic Medical Devices - Measurement of Quantities in Samples of Biological Origin - Description of Reference Materials
EN 12286:1998 In Vitro Diagnostic Medical Devices - Measurement of Quantities in Samples of Biological Origin - Presentation of Reference Measurement Procedures (Incorporates Amendment A1: 2000)

AT-ON, In vitro degradation reference

ONR CEN/TS 17405-2020 Stationary source emissions - Determination of the volume concentration of carbon dioxide - Reference method: infrared spectrometry (CEN/TS 17405:2020)
OENORM EN ISO 16256:2021 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/DIS 16256:2021)

AENOR, In vitro degradation reference

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)
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)
UNE-EN ISO 20776-1:2007 Clinical laboratory testing and in vitro diagnostic test systems - Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices - Part 1: Reference method for testing the in vitro activity of antim
UNE-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)

IX-EU/EC, In vitro degradation reference

M 348-2004 STANDARDISATION MANDATE TO CEN FOR UPDATING NATIONAL TEST METHODS RELATED TO THE BIODEGRADABILITY OF SURFACTANTS

ES-UNE, In vitro degradation reference

UNE-EN ISO 16256:2021 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) (Endorsed by Asociac...

未注明发布机构, In vitro degradation reference

DIN EN ISO 16256:2022 Laboratory medical examinations and in vitro diagnostic systems – Broth microdilution reference method for testing the in vitro activity of antimicrobial substances against budding fungi that cause infectious diseases
BS EN ISO 15193:2009(2016) In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Requirements for content and presentation of reference measurement procedures

国家市场监督管理总局、中国国家标准化管理委员会, In vitro degradation reference

GB/T 19702-2021 In vitro diagnostic medical devices—Measurement of quantities in samples of biological origin—Requirements for content and presentation of reference measurement procedures
GB/T 19703-2020 In vitro diagnostic medical devices—Measurement of quantities in samples of biological origin—Requirements for certified reference materials and the content of supporting documentation

GOSTR, In vitro degradation reference

GOST R ISO 20776-1-2010 Clinical laboratory testing and in vitro diagnostic test systems. Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices. Part 1. Reference method for testing the in vitro activity of antimic