Plasma fibrinolysis process

Plasma fibrinolysis process, Total:91 items.

The international standard classification for "Plasma fibrinolysis process" includes: Implants for surgery, prosthetics and orthotics , Surgical instruments and materials .

The Chinese standard classification for "Plasma fibrinolysis process" includes: Extracorporeal circulation, artificial organ and prosthesis device , Medical apparatus and devices in general .

国家药监局

YY 0465-2019 Disposable membrane plasmaseparator and plasma component separator

Professional Standard - Agriculture

592药典化学药和生物制品卷-2010 Chapter 8 Medications for the Blood System Section 2 Hemostatic and Antifibrinolytic Drugs 1. The hemostatic drug menadione acetate
598药典化学药和生物制品卷-2010 Chapter VIII Drugs for Blood System Section II Hemostatic and Antifibrinolytic Drugs I. Hemostatic Drug Human Fibrinogen
599药典化学药和生物制品卷-2010 Chapter VIII Drugs for Blood System Section II Hemostatic and Antifibrinolytic Drugs I. Hemostatic Drug Human Prothrombin Complex
601药典化学药和生物制品卷-2010 Chapter VIII Medications for the Blood System Section 2 Hemostasis and Antifibrinolytic Drugs 2. Antifibrinolytic Drug Aminomethylbenzoic Acid
589药典化学药和生物制品卷-2010 Chapter 8 Medications for Blood System Section 2 Hemostatic and Antifibrinolytic Drugs 1. Hemostatic Drug Vitamin K
590药典化学药和生物制品卷-2010 Chapter 8 Medications for Blood System Section 2 Hemostasis and Antifibrinolytic Drugs 1. Hemostatic Drugs Vitamin K1
595药典化学药和生物制品卷-2010 Chapter VIII Medications for the Blood System Section II Hemostatic and Antifibrinolytic Drugs I. Hemostatic Drugs Human Coagulation Factor Ⅷ
602药典化学药和生物制品卷-2010 Chapter VIII Medications for the Blood System Section 2 Hemostasis and Antifibrinolytic Drugs 2. Antifibrinolytic Drug Etamsulfame
594药典化学药和生物制品卷-2010 Chapter 8 Medications for the Blood System Section 2 Hemostatic and Antifibrinolytic Drugs 1. Hemostatic Drug Coagulation Factor
600药典化学药和生物制品卷-2010 Chapter VIII Blood System Drugs Section 2 Hemostasis and Antifibrinolytic Drugs 2. Antifibrinolytic Drug Tranexamic Acid
596药典化学药和生物制品卷-2010 Chapter VIII Blood System Medications Section II Hemostatic and Antifibrinolytic Drugs I. Hemostatic Drugs Recombinant Human Coagulation Factor Ⅷ

Professional Standard - Medicine

YY 0465-2003 Single use membrane plasmaseparator
YY 0465-2009 Disposable membrane plasmaseparator

General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China

GB/T 43279.3-2023 Molecular in vitro diagnostic examinations—Specifications for pre-examination processes for venous whole blood—Part 3: Isolated circulating cell free DNA from plasma

Group Standards of the People's Republic of China

T/CSRME 003-2020 Technical specification for karst grouting engineering

未注明发布机构

DIN EN ISO 20186-3 E:2018-02 Procedure Specification for Preliminary Examination of Venous Whole Blood for Molecular In Vitro Diagnostic Examination Part 3: Isolation of Circulating Cell-Free DNA from Plasma (Draft)

RU-GOST R

GOST 16445-1978 Haemolytic serum for the compliment fixation test. Specifications
GOST 11006-1974 Rayon grade pulp. Method for the determination of time for filtration of caustic soda solution through alkalinous cellulose

British Standards Institution (BSI)

BS ISO 8637-3:2024 Extracorporeal systems for blood purification - Plasmafilters
BS EN ISO 23118:2021 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
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
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 446:1997 Grout for prestressing tendons - Grouting procedures

GSO

GSO ISO 13960:2015 Cardiovascular implants and extracorporeal systems -- Plasmafilters
GSO ISO 23118:2023 Molecular in vitro diagnostic examinations — Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
BH GSO ISO 23118:2023 Molecular in vitro diagnostic examinations — Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma

Korean Agency for Technology and Standards (KATS)

KS P ISO 13960:2017 Cardiovascular implants and extracorporeal systems — Plasmafilters
KS P ISO 13960:2010 Cardiovascular implants and artificial organs-Plasmafilters
KS P ISO 20186-3-2023 Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 3: Isolated circulating cell free DNA from plasma

International Organization for Standardization (ISO)

ISO 13960:2003 Cardiovascular implants and artificial organs - Plasmafilters
ISO 13960:2010 Cardiovascular implants and extracorporeal systems - Plasmafilters
ISO 8637-3:2024 Extracorporeal systems for blood purification — Part 3: Plasmafilters
ISO 8637-3:2018 Extracorporeal systems for blood purification - Part 3: Plasmafilters
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

RO-ASRO

STAS 11326/6-1985 RUBBER STOPPERS FOR BLOOD, PLASMA AND A QUEOUS SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS Inocuity checking up
STAS 11326/3-1984 RUBBER STOPPERS FOR INJECTABLE AND PERFUSABLE BLOOD, PLASMA AND AQUEOUS SOLUTION BOTTLES Toxicity checking up
STAS 11327/3-1983 RUBBER STOPPERS FOR BLOOD,PLASMA AND SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS pH aqueous extract checking out
STAS 11326/2-1985 RUBBER STOPPERS FOR BLOOD, PLASMA AND AQUEOUS SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS Pyrogenic impurities checking up
STAS 8938-1971 PULPS Determination of the reactivity of chemical pulps through the solubility in cadoxen
STAS 11327/9-1983 RUBBER STOPPERS FOR BLOOD, PLASMA AND SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS Organic substances determination
STAS 11327/2-1983 RUBBER STOPPERS FOR BLOOD, PLASMA AND SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS Apparence, smell and taste checking out
STAS 11326/4-1984 RUBBER STOPPERS FOR RECIPIENTS OF BLOOD, PLASMA AND AQUEOUS SOLUTIONS FOR INJECTIONS AND PERFUSIONS Hcmolityc impurities checking up
STAS 11327/8-1983 RUBBER STOPPERS FOR BLOOD,PLASMA AND SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS etermination of volatile sulphides
STAS 11326/8-1985 RUBBER STOPPERS FOR BLOOD, PLASMA AND INJECTABLE AND PERFUSABLE AQUEOUS SOLUTIONS Microbiological checking up of poisonous substances with antibacterian action
STAS 11327/4-1983 RUBBER STOPPERS FOR BLOOD, PLASMA AND SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS Determination of oxidoreduction substances of aqueous extract
STAS 11327/5-1983 RUBBER STOPPERS FOR BLOOD, PLASMA AND SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS Determination of heavy metals and zinc of aqueous extract
STAS 12343-1985 Fibrous half-stuffs of pulpy industry POLLUTION DEGREE DETERMINATION
STAS 6209-1967 Semi-finished fiber products for pulp industry. Determination of solubility in sodium hydroxide solvent

KR-KS

KS P ISO 8637-3-2022 Extracorporeal systems for blood purification Part 3: Plasmafilters

SCC

BS PD CEN/TS 16945:2016 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for metabolomics in urine, venous blood serum and plasma
DANSK DS/ISO 23118:2021 Molecular in vitro diagnostic examinations – Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
DANSK DS/CEN/TS 16945:2016 Molecular in vitro diagnostic examinations – Specifications for pre-examination processes for metabolomics in urine, venous blood serum and plasma
SN-CEN/TS 16945:2016 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for metabolomics in urine, venous blood serum and plasma
DANSK DS/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
NS-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)
BS PD CEN/TS 16835-3:2015 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for venous whole blood-Isolated circulating cell free DNA from plasma
DANSK DS/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)
BS 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
SN-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
DIN 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; German version CEN/TS 17742:2022
CSA ISO 20186-3:2022 Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 3: Isolated circulating cell free DNA from plasma
SN-CEN/TS 16835-3:2015 Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 3: Isolated circulating cell free DNA from plasma
DANSK DS/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
DANSK DS/CEN/TS 16835-3:2015 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 3: Isolated circulating cell free DNA from plasma

Association Francaise de Normalisation

NF EN ISO 23118:2021 In Vitro Molecular Diagnostic Assays - Preanalytical Process Specifications for Metabolome Analysis in Urine and Venous Blood (Serum and 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 S93-306:1992 Extracorporeal circuits. Sterile, single-use units for filtration plasma separators (single-use, sterile plasmafilters).
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

German Institute for Standardization

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 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 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 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

IT-UNI

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

ES-UNE

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)

Danish Standards Foundation

DS/ISO 23118:2021 Molecular in vitro diagnostic examinations – Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma

European Committee for Standardization (CEN)

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
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
prEN ISO 18703 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)

AT-ON

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)

Lithuanian Standards Office

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)

CH-SNV

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)

GOST

GOST R ISO 23118-2023 Molecular in vitro diagnostic examinations. Requirements for the processes of the preanalytical stage of the study of the metabolomics of urine, serum and plasma of venous blood

American Society for Testing and Materials (ASTM)

ASTM F1841-97(2005) Standard Practice for Assessment of Hemolysis in Continuous Flow Blood Pumps
ASTM F1841-19e1 Standard operating procedure for assessment of hemolysis in continuous flow blood pumps

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