ZH
RU
ES

plasmaserumfor in vitro diagnostic

plasmaserumfor in vitro diagnostic, Total:154 items.

In the international standard classification, plasmaserumfor in vitro diagnostic involves: Laboratory medicine, Medical equipment, Applications of information technology, Medical sciences and health care facilities in general, Microbiology.

Association Francaise de Normalisation, plasmaserumfor in vitro diagnostic

NF EN ISO 23118:2021 Analyses de diagnostic moléculaire in vitro - Spécifications relatives aux processus préanalytiques pour l'analyse du métabolome dans l'urine et le sang veineux (sérum et plasma)
NF S62-084*NF EN ISO 23118:2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
NF S92-075-3*NF EN ISO 20186-3:2019 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 3 : isolated circulating cell free DNA from plasma
NF EN ISO 20186-3:2019 Analyses de diagnostic moléculaire in vitro - Spécifications relatives aux processus préanalytiques pour le sang total veineux - Partie 3 : ADN libre circulant extrait du plasma
NF S92-036:2004 In vitro diagnostic medical devices - Single-use receptables for the collection of specimens, other than blood, from humans.
NF S92-036*NF EN ISO 6717:2021 In vitro diagnostic medical devices - Single-use containers for the collection of specimens from humans other than blood
NF EN ISO 6717:2021 Dispositifs médicaux de diagnostic in vitro - Récipients à usage unique pour le prélèvement d'échantillons d'origine humaine autres que le sang
NF S92-026:2004 In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus.
NF S92-026:2013 In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus
NF S92-026*NF EN ISO 15197:2015 In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus
NF S92-075-1*NF EN ISO 20186-1:2019 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1 : isolated cellular RNA
XP S92-075-1*XP CEN/TS 16835-1:2015 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1 : isolated cellular RNA
NF EN ISO 20186-1:2019 Analyses de diagnostic moléculaire in vitro - Spécifications relatives aux processus préanalytiques pour le sang total veineux - Partie 1 : ARN cellulaire extrait
NF S92-075-2*NF EN ISO 20186-2:2019 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2 : isolated genomic DNA
XP S92-075-2*XP CEN/TS 16835-2:2015 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2 : isolated genomic DNA
NF EN ISO 15197:2015 Systèmes d'essais de diagnostic in vitro - Exigences relatives aux systèmes d'autosurveillance de la glycémie destinés à la prise en charge du diabète sucré
NF EN ISO 20186-2:2019 Analyses de diagnostic moléculaire in vitro - Spécifications relatives aux processus préanalytiques pour le sang total veineux - Partie 2 : ADN génomique extrait

Danish Standards Foundation, plasmaserumfor in vitro diagnostic

DS/ISO 23118:2021 Molecular in vitro diagnostic examinations – Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
DS/ISO 6717:2021 In vitro diagnostic medical devices – Single-use containers for the collection of specimens from humans other than blood
DS/EN ISO 15197:2013 In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus

IT-UNI, plasmaserumfor in vitro diagnostic

UNI EN ISO 23118:2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
UNI CEN/TS 17390-1-2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood - Part 1: Isolated RNA
UNI CEN/TS 17390-2-2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood - Part 2: Isolated DNA

European Committee for Standardization (CEN), plasmaserumfor in vitro diagnostic

PD CEN/TS 16945:2016 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for metabolomics in urine@ venous blood serum and plasma
EN ISO 23118:2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma (ISO 23118:2021)
FprCEN/TS 17742-2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free RNA from plasma
prEN ISO 18703 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free RNA from plasma
CEN/TS 17742:2022 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free RNA from plasma
EN ISO 20186-3:2019 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)
EN ISO 6717:2021 In vitro diagnostic medical devices - Single-use containers for the collection of specimens from humans other than blood (ISO 6717:2021)
EN 14254:2004 In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humans
PD CEN/TS 16835-3:2015 Molecular in vitro diagnostic e xaminations - Specifications for pre-examination processes for venous whole blood - Part 3: Isolated circulating cell free DNA from plasma
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)
EN ISO 15197:2003 In vitro diagnostic test systems Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus ISO 15197:2003
EN ISO 15197:2013 In vitro diagnostic test systems - Requirements for bloodglucose monitoring systems for self-testing in managing diabetes mellitus
FprCEN/TS 17747-2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for exosomes and other extracellular vesicles in venous whole blood - DNA, RNA and proteins
prCEN ISO/TS 18702 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for exosomes and other extracellular vesicles in venous whole blood - DNA, RNA and proteins
CEN/TS 17747:2022 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for exosomes and other extracellular vesicles in venous whole blood - DNA, RNA and proteins
PD CEN/TS 16835-1:2015 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1: Isolated cellular RNA
PD CEN/TS 16835-2:2015 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2: Isolated genomic DNA
CEN/TS 17390-2:2020 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood - Part 2: Isolated DNA
CEN/TS 17390-1:2020 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood - Part 1: Isolated RNA

ES-UNE, plasmaserumfor in vitro diagnostic

UNE-EN ISO 23118:2022 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma (ISO 23118:2021)
UNE-CEN/TS 17742:2022 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free RNA from plasma (Endorsed by Asociación Española de Normalización in May of 2022.)
UNE-EN ISO 20186-3:2020 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)
UNE-EN ISO 6717:2022 In vitro diagnostic medical devices - Single-use containers for the collection of specimens from humans other than blood (ISO 6717:2021)
UNE-EN ISO 20186-1:2019 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1: Isolated cellular RNA (ISO 20186-1:2019)
UNE-CEN/TS 17747:2022 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for exosomes and other extracellular vesicles in venous whole blood - DNA, RNA and proteins (Endorsed by Asociación Española de Normalización in June of 2022.)
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)
UNE-EN ISO 20186-2:2020 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2: Isolated genomic DNA (ISO 20186-2:2019)

German Institute for Standardization, plasmaserumfor in vitro diagnostic

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
DIN EN ISO 23118:2020 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma (ISO/DIS 23118:2020); German and English version prEN ISO 23118:2020
DIN EN ISO 23118:2021 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
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
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
DIN EN ISO 20186-3:2020 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)
DIN EN 14254:2004 In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humans; German version EN 14254:2004
DIN EN ISO 6717:2020 In vitro diagnostic medical devices - Single-use containers for the collection of specimens, other than blood, from humans (ISO/DIS 6717:2020); German and English version prEN ISO 6717:2020
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
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
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
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 / Note: DIN EN ISO 15197 (2013-11) remains valid alongside this stand...
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
DIN EN ISO 20186-1:2019 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1: Isolated cellular RNA (ISO 20186-1:2019)
DIN EN ISO 6717:2021 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
DIN 58969-10:2003 Medical microbiology - Diagnostics of infectious diseases in serological and molecular biology - Part 10: Complement fixation test (CFT)
DIN EN ISO 20186-2:2019 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2: Isolated genomic DNA (ISO 20186-2:2019)
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
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
DIN 58968-20:1990 Immunology; serodiagnosis of immune diseases; indirect immunofluorescence test, special requirements for the detection of autoantibodies
DIN 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); German version EN ISO 15197:2015
DIN EN ISO 15197:2013 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 15197:2013

Professional Standard - Agriculture, plasmaserumfor in vitro diagnostic

163药典三部-2015 Monograph ⅣIn vitro diagnosis of syphilitic rapid plasma reagin diagnostic reagents
137药典三部-2010 Each monograph catalog Ⅳ in vitro diagnosis of syphilis rapid plasma reagin diagnostic reagents
140药典三部-2010 Chapter Ⅳ In vitro diagnostic anti-A and anti-B blood typing reagents (human serum)
164药典三部-2015 Monograph IV In vitro diagnosis of syphilis Toluidine red unheated serum test diagnostic reagents
117兽药产品说明书范本第三册-2013 Diagnostic product chlamydiosis indirect hemagglutination test antigen, positive serum and negative serum instructions
133兽药典三部-2015 Text Table of Contents Diagnostic Products Chlamydiosis Indirect Hemagglutination Test Antigen, Positive Serum and Negative Serum
138药典三部-2010 Items of each monograph Ⅳ In vitro diagnosis of syphilis Toluidine red unheated serum test diagnostic reagents
94兽药产品说明书范本第三册-2013 Diagnostic products Mycoplasma gallisepticum tiger red serum plate agglutination test antigen, positive serum and negative serum instructions
116兽药产品说明书范本第三册-2013 Diagnostic product chlamydiosis complement fixation test antigen, positive serum and negative serum instructions
107兽药典三部-2015 Text Contents Diagnostic Products Mycoplasma Gallisepticum Tiger Red Serum Plate Agglutination Test Antigen, Positive Serum and Negative Serum
95兽药产品说明书范本第三册-2013 Diagnostic products Mycoplasma gallisepticum crystal violet serum plate agglutination test antigen, positive serum and negative serum instructions
83兽药产品说明书范本第三册-2013 Instructions for diagnostic products melioid complement fixation test antigen, positive serum and negative serum
123兽药产品说明书范本第三册-2013 Instructions for Microindirect Hemagglutination Test Antigen, Positive Serum and Negative Serum for Diagnostic Products of Mycoplasma Pneumoniae
108兽药典三部-2015 Text Contents Diagnostic Products Mycoplasma Gallisepticum Crystal Violet Serum Plate Agglutination Test Antigen, Positive Serum and Negative Serum
132兽药典三部-2015 Text Table of Contents Diagnostic Products Chlamydia Complement Fixation Test Antigen, Positive Serum and Negative Serum
97兽药典三部-2015 Text Contents Diagnostic Products Melioidosis Complement Fixation Test Antigen, Positive Serum and Negative Serum
139兽药典三部-2015 Text Contents Diagnostic Products Mycoplasma Pneumonia Micro-indirect Hemagglutination Test Antigen, Positive Serum and Negative Serum
85兽药产品说明书范本第三册-2013 Diagnostic products Brucellosis complement fixation test antigen, positive serum and negative serum instructions
103兽药产品说明书范本第三册-2013 Diagnostic product bovine paratuberculosis complement fixation test antigen, positive serum and negative serum instructions
99兽药典三部-2015 Text Table of Contents Diagnostic Products Brucellosis Complement Fixation Test Antigen, Positive Serum and Negative Serum
119兽药典三部-2015 Text Contents Diagnostic Products Bovine Paratuberculosis Complement Fixation Test Antigen, Positive Serum and Negative Serum
114兽药产品说明书范本第三册-2013 Diagnostic products trypanosomiasis evangelia complement fixation test antigen, positive serum and negative serum instructions
104兽药产品说明书范本第三册-2013 Diagnostic products Bovine and sheep paratuberculosis complement fixation test antigen, positive serum and negative serum instructions
120兽药典三部-2015 Text Contents Diagnostic Products Bovine and Sheep Paratuberculosis Complement Fixation Test Antigen, Positive Serum and Negative Serum
130兽药典三部-2015 Main text Table of Contents Diagnostic products Trypanosomiasis complement fixation test antigen, positive serum and negative serum
102兽药产品说明书范本第三册-2013 Instructions for Bovine Infectious Pleuropneumonia Complement Fixation Test Antigen, Positive Serum and Negative Serum for Diagnostic Products
118兽药典三部-2015 Text Contents Diagnostic Products Bovine Infectious Pleuropneumonia Complement Fixation Test Antigen, Positive Serum and Negative Serum
165药典三部-2015 Monograph IV In Vitro Diagnostic Anti-A Anti-B Blood Typing Reagents (Monoclonal Antibodies)
184药典三部-2020 Monograph IV In Vitro Diagnostic Anti-A Anti-B Blood Typing Reagents (Monoclonal Antibodies)
139药典三部-2010 Each monograph catalog Ⅳ in vitro diagnostic anti-A anti-B blood typing reagent (monoclonal antibody)

International Organization for Standardization (ISO), plasmaserumfor in vitro diagnostic

ISO 23118:2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
ISO 20186-3:2019 Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 3: Isolated circulating cell free DNA from plasma
ISO 6717:2021 In vitro diagnostic medical devices - Single-use containers for the collection of specimens from humans other than blood
ISO 15197:2013 In vitro diagnostic test systems.Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus
ISO 15197:2003 In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus
ISO 20186-1:2019 Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 1: Isolated cellular RNA
ISO/IEEE 11073-10417:2010 Health informatics - Personal health device communication - Part 10417: Device specialization - Glucose meter
ISO 20186-2:2019 Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 2: Isolated genomic DNA

AT-ON, plasmaserumfor in vitro diagnostic

OENORM EN ISO 23118:2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma (ISO 23118:2021)

CH-SNV, plasmaserumfor in vitro diagnostic

SN EN ISO 23118:2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma (ISO 23118:2021)
SN EN ISO 6717:2021 In vitro diagnostic medical devices - Single-use containers for the collection of specimens from humans other than blood (ISO 6717:2021)

Lithuanian Standards Office , plasmaserumfor in vitro diagnostic

LST EN ISO 23118:2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma (ISO 23118:2021)
LST EN ISO 15197:2004 In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2003)
LST EN ISO 15197:2004/AC:2005 In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2003)

British Standards Institution (BSI), plasmaserumfor in vitro diagnostic

BS EN ISO 23118:2021 Tracked Changes. Molecular in vitro diagnostic examinations. Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
20/30375467 DC BS EN ISO 23118. Molecular in vitro diagnostic examinations. Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
BS EN ISO 20186-3:2019 Molecular in-vitro diagnostic examinations. Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free DNA from plasma
PD CEN/TS 17742:2022 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for venous whole blood. Isolated circulating cell free RNA from plasma
BS EN ISO 20186-1:2019 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for venous whole blood - Isolated cellular RNA
BS EN ISO 20186-2:2019 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for venous whole blood - Isolated genomic DNA
BS EN 14254:2004 In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humans
20/30424657 DC BS EN ISO 6717. In vitro diagnostic medical devices. Single-use containers for the collection of specimens, other than blood, from humans
BS EN ISO 15197:2003 In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus
BS EN ISO 15197:2013 In vitro diagnostic test systems. Requirements for blood-glucosemonitoring systems for self-testing in managing diabetes mellitus
BS EN ISO 6717:2021 Tracked Changes. In vitro diagnostic medical devices. Single-use containers for the collection of specimens from humans other than blood
PD CEN/TS 17747:2022 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for exosomes and other extracellular vesicles in venous whole blood. DNA, RNA and proteins
PD CEN/TS 17390-2:2020 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood. Isolated DNA
BS EN ISO 15197:2015 Tracked Changes. In vitro diagnostic test systems. Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus
PD CEN/TS 17390-1:2020 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood. Isolated RNA
PD CEN/TS 17390-3:2020 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood. Preparations for analytical CTC staining

未注明发布机构, plasmaserumfor in vitro diagnostic

DIN EN ISO 15197:2004 Test systems for in vitro diagnostics – requirements for blood glucose measuring systems for self-use in diabetes mellitus
DIN EN 14252:2004 In-vitro diagnostics – disposable vessels for human specimens with the exception of blood samples; German version EN 14254:2004

国家市场监督管理总局、中国国家标准化管理委员会, plasmaserumfor in vitro diagnostic

GB/T 19634-2021 In vitro diagnostic test systems—General technical requirements for blood-glucose monitoring systems for self-testing

General Administration of Quality Supervision, Inspection and Quarantine of the People‘s Republic of China, plasmaserumfor in vitro diagnostic

GB/T 19634-2005 In vitro diagnostic test systems.General technical requirements for blood-glucose monitoring systems for self-testing
GB/T 19634-2005(XG1-2006) In vitro diagnostic test systems-General technical requirements for blood-glucose monitoring systems for self-testing AMD 1

GOSTR, plasmaserumfor in vitro diagnostic

GOST R EN 14254-2010 In vitro diagnostic medical devices. Single-use receptacles for the collection of specimens, other than blood, from humans
GOST ISO 15197-2011 In vitro diagnostic test systems. Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus

AENOR, plasmaserumfor in vitro diagnostic

UNE-EN 14254:2004 In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humans
UNE-EN ISO 15197:2013 In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2013)

Indonesia Standards, plasmaserumfor in vitro diagnostic

SNI ISO 15197:2009 In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus

Taiwan Provincial Standard of the People's Republic of China, plasmaserumfor in vitro diagnostic

CNS 15035-2006 In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus

Canadian Standards Association (CSA), plasmaserumfor in vitro diagnostic

CSA ISO 15197-05-CAN/CSA:2005 Syst鑝es d'essais de diagnostic in vitro ?Exigences relatives aux syst鑝es d'autosurveillance de la glyc閙ie destin閟 ?la prise en charge du diab鑤e sucr镻remi鑢e 閐ition
CAN/CSA-ISO 15197:2015 In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (Second Edition)

Korean Agency for Technology and Standards (KATS), plasmaserumfor in vitro diagnostic

KS P ISO 15197:2010 In vitro diagnostic test systems－Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus
KS P ISO 15197:2017 In vitro diagnostic test systems — Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus

RU-GOST R, plasmaserumfor in vitro diagnostic

GOST R ISO 15197-2015 In vitro diagnostic test systems. Requirements for blood glucose monitoring systems for self-testing in managing diabetes mellitus
GOST R 55991.6-2014 In vitro diagnostics medical devices. Part 6. Automatic analyzers for hematology tests. Technical requirements for public procurement

CEN - European Committee for Standardization, plasmaserumfor in vitro diagnostic

EN ISO 20186-1:2019 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1: Isolated cellular RNA
EN ISO 20186-2:2019 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2: Isolated genomic DNA

KR-KS, plasmaserumfor in vitro diagnostic

KS P ISO 15197-2017(2022) In vitro diagnostic test systems — Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus
KS P ISO 15197-2017 In vitro diagnostic test systems — Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus
KS P ISO 20186-1-2022 Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 1: Isolated cellular RNA