Tra cứu Tiêu chuẩn quốc tế
Tìm thấy 22422 kết quả.
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| 11501 |
EN ISO 10993-15Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000) Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000) |
| 11502 |
EN ISO 10993-16Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2017) Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2017) |
| 11503 |
EN ISO 10993-17Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002) Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002) |
| 11504 |
EN ISO 10993-18Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005) Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005) |
| 11505 |
EN ISO 10993-2Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO 10993-2:2006) Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO 10993-2:2006) |
| 11506 |
EN ISO 10993-3Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:2014) Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:2014) |
| 11507 |
EN ISO 10993-4Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2017) Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2017) |
| 11508 |
EN ISO 10993-5Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009) Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009) |
| 11509 |
EN ISO 10993-6Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2016) Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2016) |
| 11510 |
EN ISO 10993-7Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2008) Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2008) |
| 11511 |
EN ISO 10993-7/ACBiological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals; Technical Corrigendum 1 (ISO 10993-7:2008/Cor 1:2009) Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals; Technical Corrigendum 1 (ISO 10993-7:2008/Cor 1:2009) |
| 11512 |
EN ISO 10993-7/prA1Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals - Amendment 1 (ISO 10993-7/DAM 1:2018) Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals - Amendment 1 (ISO 10993-7/DAM 1:2018) |
| 11513 |
EN ISO 10993-9Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:2009) Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:2009) |
| 11514 |
EN ISO 1101Geometrical product specifications (GPS) - Geometrical tolerancing - Tolerances of form, orientation, location and run-out (ISO 1101:2017) Geometrical product specifications (GPS) - Geometrical tolerancing - Tolerances of form, orientation, location and run-out (ISO 1101:2017) |
| 11515 |
EN ISO 11011Compressed air - Energy efficiency - Assessment (ISO 11011:2013) Compressed air - Energy efficiency - Assessment (ISO 11011:2013) |
| 11516 |
EN ISO 11052Durum wheat flour and semolina - Determination of yellow pigment content (ISO 11052:1994) Durum wheat flour and semolina - Determination of yellow pigment content (ISO 11052:1994) |
| 11517 |
EN ISO 11058Geotextiles and geotextile-related products - Determination of water permeability characteristics normal to the plane, without load (ISO 11058:2010) Geotextiles and geotextile-related products - Determination of water permeability characteristics normal to the plane, without load (ISO 11058:2010) |
| 11518 |
EN ISO 11063Soil quality - Method to directly extract DNA from soil samples (ISO 11063:2012) Soil quality - Method to directly extract DNA from soil samples (ISO 11063:2012) |
| 11519 |
EN ISO 11064-1Ergonomic design of control centres - Part 1: Principles for the design of control centres (ISO 11064-1:2000) Ergonomic design of control centres - Part 1: Principles for the design of control centres (ISO 11064-1:2000) |
| 11520 |
EN ISO 11064-2Ergonomic design of control centres - Part 2: Principles for the arrangement of control suite (ISO 11064-2:2000) Ergonomic design of control centres - Part 2: Principles for the arrangement of control suite (ISO 11064-2:2000) |
