ISO 10993-1:2009
$46.15
Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management process
Published By | Publication Date | Number of Pages |
ISO | 2009-10 | 28 |
If you have any questions, feel free to reach out to our online customer service team by clicking on the bottom right corner. We’re here to assist you 24/7.
Email:[email protected]
ISO 10993-1:2009 describes:
- the general principles governing the biological evaluation of medical devices within a risk management process;
- the general categorization of devices based on the nature and duration of their contact with the body;
- the evaluation of existing relevant data from all sources;
- the identification of gaps in the available data set on the basis of a risk analysis;
- the identification of additional data sets necessary to analyse the biological safety of the medical device;
- the assessment of the biological safety of the medical device.
Published Code | ISO |
---|---|
Published By | International Organization for Standardization |
Publication Date | 2009-10 |
Pages Count | 28 |
Language | English |
Edition | 4 |
File Size | 696.3 KB |
ICS Codes | 11.100.20 - Biological evaluation of medical devices |
Related products
-
BS EN ISO 10993-17:2002:2003 Edition
Biological evaluation of medical devices – Establishment of allowable limits for leachable substances Published By…
-
AAMI 10993 5 2009 RA 2014
ANSI/AAMI/ISO 10993-5:2009/(R)2014 – Biological evaluation of medical devices-Part 5: Tests for in vitro cytotoxicity Published…
-
ISO 7237:1993/Amd 1:2001
Caravanes — Masses et dimensions — Vocabulaire — Amendement 1 Published By Publication Date Number…
-
BS EN ISO 10993-14:2009
Biological evaluation of medical devices – Identification and quantification of degradation products from ceramics Published…
-
ASTM-F2808 2010
F2808-10 Standard Test Method for Performing Behind-the-Knee (BTK) Test for Evaluating Skin Irritation Response to…
-
AAMI 10993 9 2009 RA 2014
ANSI/AAMI/ISO 10993-9:2009/(R)2014 – Biological evaluation of medical devices, Part 9: Framework for identification and quantification…
-
AAMI TIR37137 2014
ANSI/AAMI/ISO TIR37137:2014 – Cardiovascular biological evaluation of medical devices-Guidance for absorbable implants Published By Publication…
-
BS EN ISO 10993-3:2003
Biological evaluation of medical devices – Tests for genotoxicity, carcinogenicity and reproductive toxicity Published By…
-
BS EN ISO 10993-12:2009
Biological evaluation of medical devices – Sample preparation and reference materials Published By Publication Date…
-
BS EN ISO 10993-3:2009
Biological evaluation of medical devices – Tests for genotoxicity, carcinogenicity and reproductive toxicity Published By…
-
ISO 6107-3:1993/Amd 1:2001
Water quality — Vocabulary — Part 3: — Amendment 1 Published By Publication Date Number…
-
BS EN ISO 10993-11:2009
Biological evaluation of medical devices – Tests for systemic toxicity Published By Publication Date Number…
-
BS EN ISO 10993-16:2009
Biological evaluation of medical devices – Toxicokinetic study design for degradation products and leachables Published…
-
ISO 3767-4:1993/Amd 1:2000
Tractors, machinery for agriculture and forestry, powered lawn and garden equipment — Symbols for operator…
-
BS EN ISO 10993-4:2017
Biological evaluation of medical devices – Selection of tests for interactions with blood Published By…
-
ISO 10998:2008/Amd 1:2014
Agricultural tractors — Requirements for steering — Amendment 1 Published By Publication Date Number of…
-
BS EN ISO 10993-1:October 2009:2017 Edition
Biological evaluation of medical devices – Evaluation and testing within a risk management process Published…
-
BS EN ISO 10993-10:2002:2006 Edition
Biological evaluation of medical devices – Tests for irritation and delayed-type hypersensitivity Published By Publication…
-
ISO 10533:1993/Amd 1:2005
Earth-moving machinery — Lift-arm support devices — Amendment 1 Published By Publication Date Number of…
-
BS EN ISO 10993-6:2009
Biological evaluation of medical devices – Tests for local effects after implantation Published By Publication…
-
BS EN ISO 10993-14:2001:2002 Edition
Biological evaluation of medical devices – Identification and quantification of degradation products from ceramics Published…
-
BS EN ISO 10993-1:June 2009:2010 Edition
Biological evaluation of medical devices – Evaluation and testing Published By Publication Date Number of…
-
BS EN ISO 10993-18:2009
Biological evaluation of medical devices – Chemical characterization of materials Published By Publication Date Number…
-
ASTM-F2808 2023
F2808-23 Standard Test Method for Performing Behind-the-Knee (BTK) Test for Evaluating Skin Irritation Response to…
-
BS EN ISO 10993-15:2009
Biological evaluation of medical devices – Identification and quantification of degradation products from metals and…
-
BS EN ISO 10993-7:2008:2010 Edition
Biological evaluation of medical devices – Ethylene oxide sterilization residuals Published By Publication Date Number…
-
ASTM-F2808 2017
F2808-17 Standard Test Method for Performing Behind-the-Knee (BTK) Test for Evaluating Skin Irritation Response to…
-
ISO 6107-8:1993/Amd 1:2001
Qualité de l’eau — Vocabulaire — Partie 8: — Amendement 1 Published By Publication Date…
-
ASTM-F2808 2017(Redline)
F2808-17 Standard Test Method for Performing Behind-the-Knee (BTK) Test for Evaluating Skin Irritation Response to…
-
BS EN ISO 10993-4:2002:2006 Edition
Biological evaluation of medical devices – Selection of tests for interactions with blood Published By…
-
BS EN ISO 10993-1:2003
Biological evaluation of medical devices – Evaluation and testing Published By Publication Date Number of…
-
BS EN ISO 10993-5:2009
Biological evaluation of medical devices – Tests for in vitro cytotoxicity Published By Publication Date…
-
BS EN ISO 10993-10:2009:2010 Edition
Biological evaluation of medical devices – Tests for irritation and delayed-type hypersensitivity Published By Publication…
-
ASTM-F2808 2023(Redline)
F2808-23 Standard Test Method for Performing Behind-the-Knee (BTK) Test for Evaluating Skin Irritation Response to…
-
BS EN ISO 10993-9:May 2009:2010 Edition
Framework for identification and quantification of potential degradation products Published By Publication Date Number of…
-
BS EN ISO 10993-17:2009
Biological evaluation of medical devices – Establishment of allowable limits for leachable substances Published By…
-
ISO 10993-4:2002/Amd 1:2006
Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood…
-
BS EN ISO 10993-9:December 2009:2010 Edition
Biological evaluation of medical devices – Framework for identification and quantification of potential degradation products…
-
ISO/IEC 11458:1993/Amd 1:2000
Information technology — Microprocessor systems — VICbus — Inter-crate cable bus — Amendment 1 Published…
-
BS EN ISO 10993-12:2007
Biological evaluation of medical devices – Sample preparation and reference materials Published By Publication Date…