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D-723-13 US Market Access And 510k Submission
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D-723-14 Complying A Multi-Country Compatible Technical File
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D-723-16 Clinical Evaluation
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D-723-19 Listing Of Medical Device In Hongkong
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D-723-20 Medical Device Registration In Taiwan
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D-723-24 Sterilization
Part 1: Basis And Terms
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D-723-25 Sterilization
Part II: Gamma Sterilization
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D-723-26 SterilizationPart III: Ethylene Oxide
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D-723-27 Sterilization
Part IV: Determination Of A Population Of Microorganisms On Products (ISO 11737-1: 2018)
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D-723-29 Design History File
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D-723-33 ISO 11607 Medical Device Packaging Validation
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D-723-36 UDI Basics For FDA And EU: Unique Device Identifier (Based on GS1 Format)
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D-723-38 Statistical Sampling Plan For Medical Device Inspection
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D-723-39 IVD Registration In Taiwan
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D-723-40 Gaining Entry To Australia
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D-723-41 EU MDR Technical File Structure
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