BSI - Health and Safety - Historical Collection
This collection contains documents from the following standards organization(s): British Standards Institution
| BSI BS EN ISO 10705-1 | EN-Water Quality - Part 1: Detection and Enumeration of Bacteriophages - Enumeration of F-Specific RNA Bacteriophages-AMD 13446: December 10 2001 | |
| BSI BS EN ISO 10939 | EN-Opthalmic Instruments - Slit-Lamp Microscopes | |
| BSI BS EN ISO 10940 | EN-Ophthalmic Instruments - Fundus Cameras | |
| BSI BS EN ISO 10942 | EN-Ophthalmic Instruments - Direct Ophthalmoscopes-CORR 13442: December 21 2001; | |
| BSI BS EN ISO 10942 | EN-Ophthalmic Instruments - Direct Ophthalmoscopes-ISO 10942: 1998; | |
| BSI BS EN ISO 10943 | EN-Ophthalmic Instruments - Indirect Ophthalmoscopes | |
| BSI BS EN ISO 10944 | EN-Ophthalmic Optics - Synoptophores | |
| BSI BS EN ISO 10993-1 | EN-Biological evaluation of medical devices Part 1: Evaluation and testing | |
| BSI BS EN ISO 10993-1 | EN-Biological evaluation of medical devices Part 1: Evaluation and testing | |
| BSI BS EN ISO 10993-1 | EN-Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process | |
| BSI BS EN ISO 10993-1 | EN-Biological Evaluation of Medical Devices Part 1: Evaluation and Testing-Supersedes BS EN 30993-1: 1994; | |
| BSI BS EN ISO 10993-1 | EN-Biological evaluation of medical devices Part 1: Evaluation and testing-CORR: April 30 2010 | |
| BSI BS EN ISO 10993-10 | EN-Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity-CORR 14275: December 20 2002; AMD 16583: September 29 2006 | |
| BSI BS EN ISO 10993-10 | EN-Biological evaluation of medical devices Part 10: Tests for irritation and delayed-type hypersensitivity | |
| BSI BS EN ISO 10993-10 | EN-Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity-CORR 14275: December 20 2002; | |
| BSI BS EN ISO 10993-10 | EN-Biological Evaluation of Medical Devices Part 10: Tests for Irritation and Sensitization | |
| BSI BS EN ISO 10993-11 | EN-Biological evaluation of medical devices Part 11: Tests for systemic toxicity | |
| BSI BS EN ISO 10993-11 | EN-Biological Evaluation of Medical Devices Part 11: Tests for Systematic Toxicity (N) | |
| BSI BS EN ISO 10993-12 | EN-Biological evaluation of medical devices - Part 12: Sample preparation and reference materials | |
| BSI BS EN ISO 10993-12 | EN-Biological evaluation of medical devices Part 12: Sample preparation and reference materials | |
| BSI BS EN ISO 10993-12 | EN-Biological Evaluation of Medical Devices Part 12: Sample Preparation and Reference Materials | |
| BSI BS EN ISO 10993-13 | EN-Biological Evaluation of Medical Devices - Part 13: Identification and Quantification of Degradation Products from Polymeric Medical Devices | |
| BSI BS EN ISO 10993-13 | EN-Biological Evaluation of Medical Devices - Part 13: Identification and Quantification of Degradation Products from Polymeric Medical Devices | |
| BSI BS EN ISO 10993-14 | EN-Biological Evaluation of Medical Devices - Part 14: Identification and Quantification of Degradation Products from Ceramics-ISO 10993-14: 2001; | |
| BSI BS EN ISO 10993-14 | EN-Biological Evaluation of Medical Devices - Part 14: Identification and Quantification of Degradation Products from Ceramics-CORR 13748: March 15 2002 | |
| BSI BS EN ISO 10993-15 | EN-Biological Evaluation of Medical Devices - Part 15: Identification and Quantification of Degradation Products from Metals and Alloys | |
| BSI BS EN ISO 10993-16 | EN-Biological Evaluation of Medical Devices Part 16: Toxicokinetic Study Design for Degradation Products and Leachables | |
| BSI BS EN ISO 10993-16 | EN-Biological evaluation of medical devices Part 16: Toxicokinetic study design for degradation products and leachables | |
| BSI BS EN ISO 10993-17 | EN-Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances | |
| BSI BS EN ISO 10993-18 | EN-Biological evaluation of medical devices Part 18: Chemical characterization of materials | |
| BSI BS EN ISO 10993-2 | EN-Biological Evaluation of Medical Devices - Part 2: Animal Welfare Requirements | |
| BSI BS EN ISO 10993-2 | EN-Biological Evaluation of Medical Devices - Part 2: Animal Welfare Requirements | |
| BSI BS EN ISO 10993-3 | EN-Biological evaluation of medical devices Part 3: Tests for genotoxicity carcinogenicity and reproductive toxicity-CORR 14920: December 23 2003; Supersedes BS EN 30993-3: 1994; | |
| BSI BS EN ISO 10993-3 | EN-Biological evaluation of medical devices Part 3: Tests for genotoxicity carcinogenicity and reproductive toxicity-Supersedes BS EN 30993-3: 1994; | |
| BSI BS EN ISO 10993-4 | EN-Biological evaluation of medical devices Part 4: Selection of tests for interactions with blood-CORR 14295: January 29 2003; AMD 16584: September 29 2006;: 1994 | |
| BSI BS EN ISO 10993-4 | EN-Biological evaluation of medical devices Part 4: Selection of tests for interactions with blood-Supersedes BS EN 30993-4: 1994; | |
| BSI BS EN ISO 10993-4 | EN-Biological evaluation of medical devices Part 4: Selection of tests for interactions with blood-CORR 14295: January 29 2003;: 1994; | |
| BSI BS EN ISO 10993-5 | EN-Biological Evaluation of Medical Devices - Part 5: Tests for In Vitro Cytotoxicity-Supersedes BS EN 30993-5:1994; | |
| BSI BS EN ISO 10993-5 | EN-Biological Evaluation of Medical Devices - Part 5: Tests for In Vitro Cytotoxicity-Supersedes BS EN 30993-5:1994; | |
| BSI BS EN ISO 10993-6 | EN-Biological evaluation of medical devices - Part 6: Tests for local effects after implantation | |
| BSI BS EN ISO 10993-7 | EN-Biological Evaluation of Medical Devices Part 7: Ethylene Oxide Sterilization Residuals (N) | |
| BSI BS EN ISO 10993-7 | EN-Biological evaluation of medical devices Part 7: Ethylene oxide sterilization residuals | |
| BSI BS EN ISO 10993-8 | EN-Biological Evaluation of Medical Devices - Part 8: Selection and Qualification of Reference Materials for Biological Tests | |
| BSI BS EN ISO 10993-9 | EN-Biological evaluation of medical devices Part 9: Framework for identification and quantification of potential degradation products-CORR: April 30 2010 | |
| BSI BS EN ISO 10993-9 | EN-Biological Evaluation of Medical Devices - Part 9: Framework for Identification and Quantification of Potential Degradation Products-AMD 10742: January 2000; | |
| BSI BS EN ISO 10993-9 | EN-Biological Evaluation of Medical Devices - Part 9: Framework for Identification and Quantification of Potential Degradation Products-AMD 10742: January 2000; | |
| BSI BS EN ISO 10993-9 | EN-Biological evaluation of medical devices Part 9: Framework for identification and quantification of potential degradation products | |
| BSI BS EN ISO 10993-9 | EN-Biological evaluation of medical devices Part 9: Framework for identification and quantification of potential degradation products | |
| BSI BS EN ISO 10993-9 | EN-Biological Evaluation of Medical Devices - Part 9: Framework for Identification and Quantification of Potential Degradation Products | |
| BSI BS EN ISO 11117 | EN-Gas cylinders - Valve protection caps and valve guards - Design construction and tests | |
| BSI BS EN ISO 11137-2 | EN-Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose | |
| BSI BS EN ISO 11138-2 | EN-Sterilization of health care products - Biological indicators - Part 2: Biological indicators for ethylene oxide sterilization processes-Supersedes BS EN 866-2: 1998 and BS EN 866-8: 2000 | |
| BSI BS EN ISO 11138-3 | EN-Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization processes-Supersedes BS EN 866-3:1997 and BS EN 866-7:2000 | |
| BSI BS EN ISO 11140-1 | EN-Sterilization of health care products Chemical indicators Part 1: General requirements-Supersedes BS EN 867-1: 1997 and BS EN 867-2:1997 | |
| BSI BS EN ISO 11140-3 | EN-Sterilization of health care products - Chemical indicators - Part 3: Class 2 indicator systems for use in the Bowie and Dick-type steam penetration test-CORR: June 30 2009 | |
| BSI BS EN ISO 11140-3 | EN-Sterilization of health care products - Chemical indicators - Part 3: Class 2 indicator systems for use in the Bowie and Dick-type steam penetration test | |
| BSI BS EN ISO 11143 | EN-Dental equipment - Amalgam separators-CORR 17321:September 282007 | |
| BSI BS EN ISO 11143 | EN-Dental Equipment - Amalgam Separators | |
| BSI BS EN ISO 11196 | EN-Anaesthetic gas monitors | |
| BSI BS EN ISO 11197 | EN-Medical supply units-Supersedes BS EN 793:1998 | |
| BSI BS EN ISO 11199-2 | EN-Walking Aids Manipulated by Both Arms - Requirements and Test Methods - Part 2: Rollators | |
| BSI BS EN ISO 11244 | EN-Dental Brazing Investments-:2006 | |
| BSI BS EN ISO 11245 | EN-Dental Restorations - Phosphate-Bonded Refractory Die Materials-:2006 | |
| BSI BS EN ISO 11246 | EN-Dental Ethyl Silicate Bonded Casting Investments-:2006 | |
| BSI BS EN ISO 11290-1 | EN-Microbiology of Food and Animal Feeding Stuffs - Horizontal Method for the Detection and Enumeration of Listeria Monocytogenes Part 1: Detection Method-Also Known as BS 5763: Part 18: 1997 | |
| BSI BS EN ISO 11334-1 | EN-Walking Aids Manipulated by One Arm - Requirements and Test Methods Part 1: Elbow Crutches-Supersedes BS 4988: 1990 | |
| BSI BS EN ISO 11348-1 | EN-Water Quality - Determination of the Inhibitory Effect of Water Samples on the Light Emission of Vibrio Fischeri (Luminescent Bacteria Test) - Part 1: Method Using Freshly Prepared Bacteria | |
| BSI BS EN ISO 11348-2 | EN-Water Quality - Determination of the Inhibitory Effect of Water Samples on the Light Emission of Vibrio Fischeri (Luminescent Bacteria Test) - Part 1: Method Using Liquid-Dried Bacteria | |
| BSI BS EN ISO 11348-3 | EN-Water Quality - Determination of the Inhibitory Effect of Water Samples on the Light Emission of Vibrio Fischeri (Luminescent Bacteria Test) - Part 3: Method Using Freeze-Dried Bacteria | |
| BSI BS EN ISO 1135-4 | EN-Transfusion equipment for medical use - Part 4: Transfusion sets for single use-CORR 16991: March 30 2007 | |
| BSI BS EN ISO 1135-4 | EN-Transfusion equipment for medical use Part 4: Transfusion sets for single use | |
| BSI BS EN ISO 11399 | EN-Ergonomics of the Thermal Environment - Principles and Application of Relevant International Standards-AMD 13444: October 29 2001; Renumbers BS ISO 11399:1995 | |
| BSI BS EN ISO 11499 | EN-Dental Cartridges for Local Anaesthetics-AMD 10696: September 1999; Renumbers BS ISO 11499: 1999 | |
| BSI BS EN ISO 11539 | EN-Ophthalmic Optics - Contact Lenses - Classification of Contact Lenses and Contact Lens Materials-:2006 | |
| BSI BS EN ISO 11553-1 | EN-Safety of machinery Laser processing machines Part 1: General safety requirements-Supersedes BS EN 12626:1997 | |
| BSI BS EN ISO 11553-2 | EN-Safety of machinery - Laser processing machines - Part 2: Safety requirements for hand-held laser processing devices | |
| BSI BS EN ISO 11607-1 | EN-Packaging for terminally sterilized medical devices Part 1: Requirements for materials sterile barrier systems and packaging systems-Supersedes BS EN 868-1: 1997 | |
| BSI BS EN ISO 11715-1 | EN-Opthalmic Optics - Format of Digital Data Files for Data Transfer for Profiling of Spectacle Lenses - Part 1: Two-Dimensional Tracers | |
| BSI BS EN ISO 11733 | EN-Water Quality - Evaluation of the Elimination and Biodegradability of Organic Compounds in an Aqueous Medium - Activated Sludge Simulation Test-AMD 10320: January 1999; Renumbers BS 6068: Section 5.20: 1996 |