Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management system (ISO 10993-1:2009); German version EN ISO 10993-1:2009
€105.42
Biological evaluation of medical devices - Part 1: Evaluation and testing (ISO 10993-1:2003); German version EN ISO 10993-1:2009.
€84.58
Standard Guide for Preservation of Tissue Engineered Medical Products (TEMPs) (Withdrawn 2013)
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Standard Test Method for Assessing Developmental Toxicity in Rats and Rabbits (Withdrawn 2010)
Standard Terminology Relating to Seized-Drug Analysis (Withdrawn 2005)
IN VITRO DIAGNOSTIC SYSTEMS. TRANSPORT PACKAGES FOR MEDICAL AND BIOLOGICAL SPECIMENS. REQUIREMENTS, TESTS.
€53.00
IN VITRO DIAGNOSTIC SYSTEMS. GUIDANCE ON THE APPLICATION OF EN 29001 And EN 46001 and of EN 29002 and EN 46002 for in vitro diagnostic medical devices.
€69.00
BIOLOGICAL EVALUATION OF MEDICAL DEVICES. PART 2: ANIMAL WELFARE REQUIREMENTS. (ISO 10993-2:1992).
€58.00
BIOLOGICAL EVALUATION OF MEDICAL DEVICES. PART 12: SAMPLE PREPARATION AND REFERENCE MATERIALS. (ISO 10993-12:1996).
BIOLOGICAL EVALUATION OF MEDICAL DEVICES. PART 9: FRAMEWORK FOR IDENTIFICATION AND QUANTIFICATION OF POTENTIAL DEGRADATION PRODUCTS (ISO 10993-9:1999)
€59.00
Biological evaluation of medical devices - Part 8: Selection and qualification of reference materials for biological tests. (ISO 10993-8:2000)
Biological evaluation of medical devices. Part 10: Tests for irritation and delayed-type hypersensitivity. (ISO 10993-10:2002)
€104.00
Standard Practice for Selecting Tests for Determining the Propensity of Materials to Cause Immunotoxicity (Withdrawn 2011)
Standard Test Method for Determining Subchronic Dermal Toxicity (Withdrawn 2010)
Standard Test Method for Evaluation of Delayed Contact Hypersensitivity (Withdrawn 2010)
