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03/100426 DC : DRAFT JAN 2003

Superseded
Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

View Superseded by
superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

BS EN ISO 10993-18 - BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 18: CHEMICAL CHARACTERIZATION OF MATERIALS
Superseded date

17-11-2005

Published date

23-11-2012

Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Symbols and abbreviated terms
5 General principles
6 Characterisation procedure
  6.1 General
  6.2 Step 1 - Qualitative information
  6.3 Step 2 - Material equivalence
  6.4 Step 3 - Quantitative information
  6.5 Step 4 - Quantitative risk assessment
  6.6 Step 5 - Estimated clinical exposure to chemicals
               present
7 Chemical characterisation parameters and methods
  7.1 General
  7.2 Polymers
  7.3 Metals and alloys
  7.4 Ceramics
  7.5 Natural macromolecules
8 Reporting of data obtained
Annex A (normative) Flowchart summarising the stepwise
                    generation of chemical characterisation data
                    for use in toxicological risk assessment
      A.1 General
      A.2 Procedure
Annex B (informative) Information sources for chemical characterisation
      B.1 General
      B.2 Generic name of material
      B.3 Other nomenclature and structure formulae of polymeric
          chemicals
          B.3.1 General
          B.3.2 IUPAC nomenclature and structure formulae of
                polymeric chemicals
          B.3.3 CAS registry number, USAN, and other registry name
                and/or number
      B.4 General information concerning chemical nature of materials
      B.5 Information from the material supplier
      B.6 Chemical analysis
          B.6.1 Non-specific chemical analysis relevant to exposure
                assessment
          B.6.2 Qualitative analysis
          B.6.3 Quantitative analysis of specific toxic chemicals
                for exposure assessment
      B.7 National and international material and/or product standards
      B.8 Material master file
Annex C (informative) Principles for judging toxicological equivalency
Bibliography

BS EN ISO 10993-18

Committee
CH/194
DocumentType
Draft
PublisherName
British Standards Institution
Status
Superseded
SupersededBy

EN 12442-3 : 2000 ANIMAL TISSUES AND THEIR DERIVATIVES UTILIZED IN THE MANUFACTURE OF MEDICAL DEVICES - PART 3: VALIDATION OF THE ELIMINATION AND/OR INACTIVATION OF VIRUSES AND TRANSMISSIBLE AGENTS
ISO 5832-1:2016 Implants for surgery — Metallic materials — Part 1: Wrought stainless steel
ISO 10993-13:2010 Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devices
ISO 10993-2:2006 Biological evaluation of medical devices — Part 2: Animal welfare requirements
EN 455-3:2015 Medical gloves for single use - Part 3: Requirements and testing for biological evaluation
ISO 10993-14:2001 Biological evaluation of medical devices — Part 14: Identification and quantification of degradation products from ceramics
ISO 10993-17:2002 Biological evaluation of medical devices — Part 17: Establishment of allowable limits for leachable substances
ISO 10993-1:2009 Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process
ISO 10993-9:2009 Biological evaluation of medical devices Part 9: Framework for identification and quantification of potential degradation products
EN 12442-1 : 2000 ANIMAL TISSUES AND THEIR DERIVATIVES UTILIZED IN THE MANUFACTURE OF MEDICAL DEVICES - PART 1: ANALYSIS AND MANAGEMENT OF RISK
ISO 14971:2007 Medical devices Application of risk management to medical devices
EN 12442-2 : 2000 ANIMAL TISSUES AND THEIR DERIVATIVES UTILIZED IN THE MANUFACTURE OF MEDICAL DEVICES - PART 2: CONTROLS ON SOURCING, COLLECTION AND HANDLING

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