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DIN Media GmbH Standards
Total Record : 19857
DIN EN ISO 10943 : 2011
Ophthalmic instruments - Indirect ophthalmoscopes (ISO 10943:2011)
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55.33
DIN EN ISO 10944 : 2010
Ophthalmic instruments - Synoptophores (ISO 10944:2009)
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63.55
DIN EN ISO 10960 : 2018
Rubber and plastics hoses - Assessment of ozone resistance under dynamic conditions (ISO 10960:2017)
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55.33
DIN EN ISO 10961 : 2020
Gas cylinders - Cylinder bundles - Design, manufacture, testing and inspection (ISO 10961:2019)
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126.36
DIN EN ISO 10991 : 2010
Micro process engineering - Vocabulary (ISO 10991:2009); Trilingual version EN ISO 10991:2009
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50.84
DIN EN ISO 10993-1 : 2021
Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2018, including corrected version 2018-10)
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158.60
DIN EN ISO 10993-10 : 2014
Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization (ISO 10993-10:2010)
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197.01
DIN EN ISO 10993-11 : 2018
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2017)
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145.14
DIN EN ISO 10993-12 : 2021
Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2021)
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119.44
DIN EN 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)
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103.36
DIN EN ISO 10993-14 : 2009
Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001)
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95.61
DIN EN ISO 10993-15 : 2009
Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000)
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95.61
DIN EN ISO 10993-16 : 2018
Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2017)
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103.36
DIN EN ISO 10993-17 : 2009
Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)
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126.36
DIN EN ISO 10993-18 : 2021
Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020)
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216.07
DIN EN ISO 10993-2 : 2023
Biological evaluation of medical devices - Part 2: Animal welfare requirements (ISO 10993-2:2022)
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95.61
DIN EN ISO 10993-23 : 2021
Biological evaluation of medical devices - Part 23: Tests for irritation (ISO 10993-23:2021)
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209.63
DIN 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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138.50
DIN EN ISO 10993-4 : 2017
Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2017)
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221.87
DIN EN ISO 10993-5 : 2009
Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009)
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138.50
DIN EN ISO 10993-6 : 2017
Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2016)
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138.50
DIN EN ISO 10993-7 : 2022
Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2008 + Cor 1:2009 + Amd 1:2019)
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221.87
DIN EN ISO 10993-9 : 2022
Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:2019)
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95.61
DIN EN ISO 1101 : 2017
Geometrical product specifications (GPS) - Geometrical tolerancing - Tolerances of form, orientation, location and run-out (ISO 1101:2017)
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281.31
DIN EN ISO 11011 : 2015
Compressed air - Energy efficiency - Assessment (ISO 11011:2013)
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164.39
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