CFR 40(PTS700-789) : JUL 2016
Superseded
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
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PROTECTION OF ENVIRONMENT - ENVIRONMENTAL PROTECTION AGENCY
Published date
23-11-2012
Publisher
Superseded date
11-04-2024
Superseded by
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| DocumentType |
Standard
|
| PublisherName |
Code of Federal Regulations
|
| Status |
Superseded
|
| SupersededBy | |
| Supersedes |
| ANSI/AAMI/ISO 10993-3:2014 | BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 3: TESTS FOR GENOTOXICITY, CARCINOGENICITY, AND REPRODUCTIVE TOXICITY |
| ASTM D 6823 : 2008 | Standard Specification for Commercial Boiler Fuels With Used Lubricating Oils |
| IEEE C57.147-2008 | IEEE Guide for Acceptance and Maintenance of Natural Ester Fluids in Transformers |
| ASTM E 2271 : 2005 : REV A : R2012 : EDT 1 | Standard Practice for Clearance Examinations Following Lead Hazard Reduction Activities in Dwellings, and in Other Child-Occupied Facilities |
| ASTM E 2308 : 2005 | Standard Guide for Limited Asbestos Screens of Buildings (Withdrawn 2014) |
| ASTM E 2271 : 2005 : REV A | Standard Practice for Clearance Examinations Following Lead Hazard Reduction Activities in Single-Family Dwellings and Child-Occupied Facilities |
| ASTM E 2913 : 2014 | Standard Practice for Hotplate Digestion of Lead from Composited Wipe Samples |
| ASTM E 1728 : 2016 : REDLINE | Standard Practice for Collection of Settled Dust Samples Using Wipe Sampling Methods for Subsequent Lead Determination |
| ASTM E 1605 : 2004 : R2012 | Standard Terminology Relating to Lead in Buildings |
| NFPA 70B : 2016 | RECOMMENDED PRACTICE FOR ELECTRICAL EQUIPMENT MAINTENANCE |
| BS EN ISO 16000-7:2007 | Indoor air Sampling strategy for determination of airborne asbestos fibre concentrations |
| BS EN ISO 10993-12:2012 | Biological evaluation of medical devices Sample preparation and reference materials |
| BS EN ISO 10993-3:2014 | Biological evaluation of medical devices Tests for genotoxicity, carcinogenicity and reproductive toxicity |
| UFC 3-550-07 : 2017 | UNIFIED FACILITIES CRITERIA - OPERATION AND MAINTENANCE (O&M;): EXTERIOR POWER DISTRIBUTION SYSTEMS |
| MIL-PRF-85570 Revision E:2012 | CLEANING COMPOUNDS, AIRCRAFT, EXTERIOR |
| ASTM E 2271 : 2005 | Standard Practice for Clearance Examinations Following Lead Hazard Reduction Activities in Single-Family Dwellings and Child-Occupied Facilities |
| ASTM D 6823 : 2008 : R2013 | Standard Specification for Commercial Boiler Fuels With Used Lubricating Oils |
| ASTM E 1605 : 2004 | Standard Terminology Relating to Lead in Buildings |
| IEEE C57.637-2015 | IEEE Guide for the Reclamation of Mineral Insulating Oil and Criteria for Its Use |
| ASTM E 2914 : 2014 | Standard Practice for Ultrasonic Extraction of Lead from Composited Wipe Samples |
| NFPA 820 : 2016 | FIRE PROTECTION IN WASTEWATER TREATMENT AND COLLECTION FACILITIES |
| DIN EN ISO 10993-12:2012-10 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2012) |
| I.S. EN ISO 10993-3:2014 | BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 3: TESTS FOR GENOTOXICITY, CARCINOGENICITY AND REPRODUCTIVE TOXICITY (ISO 10993-3:2014) |
| I.S. EN ISO 10993-12:2012 | BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 12: SAMPLE PREPARATION AND REFERENCE MATERIALS (ISO 10993-12:2012) |
| NBR 8371 : 2005 | ASKARELS FOR TRANSFORMERS AND CAPACITORS |
| MIL-A-81264 Base Document:1965 | Asbestos Felt or Mat, Resin Impregnated |
| ASTM E 2252 : 2018 : REDLINE | Standard Practice for Selection of Lead Hazard Reduction Methods for Identified Risks in Residential Housing or Child Occupied Facilities |
| MIL-PRF-24951 Revision B:1995 | FUEL OIL RECLAIMED |
| ASTM E 1373 : 2001 : R2005 : EDT 1 | Standard Test Method for Conducting a Subchronic Inhalation Toxicity Study in Rats (Withdrawn 2009) |
| ASTM E 1760 : 2016 : REDLINE | Standard Guide for Unrestricted Disposition of Bulk Materials Containing Residual Amounts of Radioactivity |
| DIN EN ISO 10993-3:2015-02 | BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 3: TESTS FOR GENOTOXICITY, CARCINOGENICITY AND REPRODUCTIVE TOXICITY (ISO 10993-3:2014) |
| ISO 16000-7:2007 | Indoor air — Part 7: Sampling strategy for determination of airborne asbestos fibre concentrations |
| ISO 10993-3:2014 | Biological evaluation of medical devices — Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity |
| ASTM D 6480 : 2005 : R2010 | Standard Test Method for Wipe Sampling of Surfaces, Indirect Preparation, and Analysis for Asbestos Structure Number Concentration by Transmission Electron Microscopy |
| UFC 3-810-01N : Change 1 | UNIFIED FACILITIES CRITERIA - NAVY AND MARINE CORPS ENVIRONMENTAL ENGINEERING FOR FACILITY CONSTRUCTION |
| ASTM D 4447 : 2015 : REDLINE | Standard Guide for Disposal of Laboratory Chemicals and Samples |
| ASTM E 2052 : 1999 | Standard Guide for Evaluation, Management, and Control of Lead Hazards in Facilities (Withdrawn 2008) |
| ASTM E 1373 : 2001 | Standard Test Method for Conducting a Subchronic Inhalation Toxicity Study in Rats |
| ASTM D 6480 : 2005 | Standard Test Method for Wipe Sampling of Surfaces, Indirect Preparation, and Analysis for Asbestos Structure Number Concentration by Transmission Electron Microscopy |
| ASTM E 2421 : 2015 : REDLINE | Standard Guide for Preparing Waste Management Plans for Decommissioning Nuclear Facilities |
| IEEE C57.106-2006 | IEEE Guide for Acceptance and Maintenance of Insulating Oil in Equipment |
| ISO 10993-12:2012 | Biological evaluation of medical devices — Part 12: Sample preparation and reference materials |
| EN ISO 16000-7:2007 | Indoor air - Part 7: Sampling strategy for determination of airborne asbestos fibre concentrations (ISO 16000-7:2007) |
| EN ISO 10993-3:2014 | Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:2014) |
| MIL-DTL-62547 Revision D:2010 | Valve and Cylinder Assemblies, Halon 1301 |
| EN ISO 10993-12:2012 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2012) |
| ANSI/AAMI/ISO 10993-12:2012 | BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 12: SAMPLE PREPARATION AND REFERENCE MATERIALS |
| ASTM E 2091 : 2017 : REDLINE | Standard Guide for Use of Activity and Use Limitations, Including Institutional and Engineering Controls |
| ASTM E 2121 : 2013 : REDLINE | Standard Practice for Installing Radon Mitigation Systems in Existing Low-Rise Residential Buildings |
| DIN EN ISO 16000-7:2007-11 | Indoor air - Part 7: Sampling strategy for determination of airborne asbestos fibre concentrations (ISO 16000-7:2007) |
| UNE-EN ISO 10993-12:2013 | Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2012) |
| UNE-EN ISO 10993-3:2015 | Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:2014) |
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