Corrigenda to DIN EN ISO 10993-1:1998-06
€0.00
Biological evaluation of medical devices Part 2: Animal welfare requirements
€77.00
Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process - Amendment 1: Determination of the uncertainty factor (ISO 10993-18:2020/Amd 1:2022)
€20.00
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for exosomes and other extracellular vesicles in venous whole blood - DNA, RNA and proteins
€142.00
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free RNA from plasma
€121.00
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for Fine Needle Aspirates (FNAs) - Part 1: Isolated cellular RNA
€163.00
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for Fine Needle Aspirates (FNAs) - Part 2: Isolated proteins
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2017)
€145.00
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for Fine Needle Aspirates (FNAs) - Part 3: Isolated genomic DNA
Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for human specimen - Isolated microbiome DNA
Standard Specification for Pipet, Blood Diluting
€58.00
Standard Specification for Glass Westergren Tube, Reusable
Implementation guidance for biorisk management for laboratories and other related organizations
€261.00
Standard Practice for Extraction of Materials Used in Medical Devices
Standard Practice for Testing Materials in Rabbits for Primary Skin Irritation