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| 81461 |
EN ISO 10938Ophthalmic optics - Chart displays for visual acuity measurement - Printed, projected and electronic (ISO 10938:2016) Ophthalmic optics - Chart displays for visual acuity measurement - Printed, projected and electronic (ISO 10938:2016) |
| 81462 |
EN ISO 10939Ophthalmic instruments - Slit-lamp microscopes (ISO 10939:2017) Ophthalmic instruments - Slit-lamp microscopes (ISO 10939:2017) |
| 81463 |
EN ISO 10940Ophthalmic instruments - Fundus cameras (ISO 10940:2009) Ophthalmic instruments - Fundus cameras (ISO 10940:2009) |
| 81464 |
EN ISO 10942Ophthalmic instruments - Direct ophthalmoscopes (ISO 10942:2006) Ophthalmic instruments - Direct ophthalmoscopes (ISO 10942:2006) |
| 81465 |
EN ISO 10943Ophthalmic instruments - Indirect ophthalmoscopes (ISO 10943:2011) Ophthalmic instruments - Indirect ophthalmoscopes (ISO 10943:2011) |
| 81466 |
EN ISO 10944Ophthalmic instruments - Synoptophores (ISO 10944:2009) Ophthalmic instruments - Synoptophores (ISO 10944:2009) |
| 81467 |
EN ISO 10960Rubber and plastics hoses - Assessment of ozone resistance under dynamic conditions (ISO 10960:2017) Rubber and plastics hoses - Assessment of ozone resistance under dynamic conditions (ISO 10960:2017) |
| 81468 |
EN ISO 10961Gas cylinders - Cylinder bundles - Design, manufacture, testing and inspection (ISO 10961:2010) Gas cylinders - Cylinder bundles - Design, manufacture, testing and inspection (ISO 10961:2010) |
| 81469 |
EN ISO 10991Micro process engineering - Vocabulary (ISO 10991:2009) Micro process engineering - Vocabulary (ISO 10991:2009) |
| 81470 |
EN ISO 10993-1Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2009) Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2009) |
| 81471 |
EN ISO 10993-1/ACBiological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process - Technical Corrigendum 1 (ISO 10993-1:2009/Cor 1:2010) Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process - Technical Corrigendum 1 (ISO 10993-1:2009/Cor 1:2010) |
| 81472 |
EN ISO 10993-10Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization (ISO 10993-10:2010) Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization (ISO 10993-10:2010) |
| 81473 |
EN ISO 10993-11Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2017) Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2017) |
| 81474 |
EN ISO 10993-12Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2012) Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2012) |
| 81475 |
EN ISO 10993-13Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:2010) Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:2010) |
| 81476 |
EN ISO 10993-14Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001) Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001) |
| 81477 |
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) |
| 81478 |
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) |
| 81479 |
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) |
| 81480 |
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) |
