I3CGlobal Clinical Evaluation January 24, 2025

Clinical Evaluation Of Reusable, Measuring and Sterile Class I Medical Devices

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I3CGlobal Clinical Evaluation January 8, 2025

How can PMS Findings Improve Device Design and Quality?

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I3CGlobal MDR / IVDR CE Marking December 26, 2024

MDR Article 17

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I3CGlobal FDA 510k November 4, 2024

FDA 510k Submission for Syringes

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I3CGlobal MDR / IVDR CE Marking September 20, 2024

Sampling of Technical Documentation

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I3CGlobal FDA 510k September 13, 2024

510k Dental Products and Material

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I3CGlobal FDA 510k August 14, 2024

510k Submissions with IEC 62304

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I3CGlobal FDA 510k August 10, 2024

FDA 510k Submission For Infusion Set

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I3CGlobal FDA 510k August 10, 2024

Required Documents for 510k submission

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