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GB/T 16886.23-2023 Biological evaluation of medical devices Part 23: Stimulation test - 英文版 |
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GB/T 16886.12-2023 Biological evaluation of Medical Devices Part 12: Sample Preparation and Reference Materials - 英文版 |
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GB/T 16886.6-2022 Biological evaluation of medical devices Part 6: local response test after implantation - 英文版 |
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GB/T 16886.4-2022 Biological evaluation of medical devices - Part 4: selection of interaction test with blood - 英文版 |
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GB/T 16886.1-2022 Biological evaluation of medical devices Part 1: evaluation and testing in the process of risk management - 英文版 |
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GB/T 16886.19-2022 Biological evaluation of medical devices - Part 19: Physicochemical, morphological and surface characterization of materials - 英文版 |
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GB/T 16886.18-2022 Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials in the risk management process - 英文版 |
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GB/T 16886.15-2022 Biological evaluation of Medical Devices-Part 15: Qualitative and Quantitative Degradation Products of Metals and Alloys - 英文版 |
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GB/T 16886.9-2022 Biological evaluation of medical devices - Part 9: Qualitative and quantitative framework for potential degradation products - 英文版 |
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GB/Z 16886.22-2022 Biological evaluation of Medical Devices Part 22: Guidelines for Nanomaterials - 英文版 |
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GB/T 16886.16-2021 Biological evaluation of medical devices—Part 16: Toxicokinetic study design for degradation products and leachables - 英文版 |
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GB/T 16886.11-2021 Biological evaluation of medical devices—Part 11:Tests for systemic toxicity - 英文版 |
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GB/T 39029-2020 Technical specification of efficacy evaluation for removing of heavy metal by biological products - 英文版 |
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GB/T 38793-2020 Technical specification of efficacy evaluation for degradation of heterocyclic pesticides by biological products - 英文版 |
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GB/T 16886.3-2019 Biological evaluation of medical devices—Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity - 英文版 |
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GB/T 27420-2018 Conformity assessment—Application guide for evaluation and expression of uncertainty in biological sample measurement - 英文版 |
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GB/T 16886.10-2017 Biological evaluation of medical devices—Part 10: Tests for irritation and skin sensitization - 英文版 |
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GB/T 16886.12-2017 Biological evaluation of medical devices—Part 12:Sample preparation and reference materials - 英文版 |
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GB/T 16886.5-2017 Biological evaluation of medical devices—Part 5: Tests for in vitro cytotoxicity - 英文版 |
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GB/T 16886.13-2017 Biological evaluation of medical devices—Part 13: Identification and quantification of degradation products from polymeric medical devices - 英文版 |
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GB/T 16886.9-2017 Biological evaluation of medical devices—Part 9: Framework for identification and quantification of potential degradation products - 英文版 |
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GB/T 33420-2016 Evaluation standard of biological for moist heat sterilization processes - 英文版 |
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GB/T 16886.6-2015 Biological evaluation of medical devices—Part 6: Tests for local effects after implantation - 英文版 |
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GB/T 16886.7-2015 Biological evaluation of medical devices—Part 7: Ethylene oxide sterilization residuals - 英文版 |
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GB/T 16886.20-2015 Biological evaluation of medical devices—Part 20: Principles and methods for immunotoxicology testing of medical devices - 英文版 |
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GB/T 16886.16-2013 Biological evaluation of medical devices―Part 16: Toxicokinetic study design for degradation products and leachables - 英文版 |
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GB/T 16886.2-2011 Biological evaluation of medical devices - Part 2: Animal welfare requirements - 英文版 |
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GB/T 16886.19-2011 Biological evaluation of medical devices - Part 19: Physico-chemical,morphological and topographical characterization of materials - 英文版 |
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GB/T 16886.18-2011 Biological evaluation of medical devices - Part 18: Chemical characterization of materials - 英文版 |
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GB/T 16886.11-2011 Biological evaluation of medical devices - Part 11: Tests for systemic toxicity - 英文版 |
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