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Surgical Instruments ( Driver Shaft ) - FDA Registration 5195c02ec8e4371d79f64b5398d46230

Access comprehensive regulatory information for Surgical Instruments ( Driver Shaft ) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 5195c02ec8e4371d79f64b5398d46230 and manufactured by Jeil Medical Corporation. The device was registered on December 29, 2021.

This page provides complete registration details including manufacturer information, authorized representative details, and regulatory compliance data from the official Myanmar FDA medical device database. Pure Global AI offers free access to Myanmar's complete medical device registry.

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5195c02ec8e4371d79f64b5398d46230
Surgical Instruments ( Driver Shaft )
FDA ID: 5195c02ec8e4371d79f64b5398d46230
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Device Classification
Brand Name
Jeil Medical
Registration Information
Analysis ID
5195c02ec8e4371d79f64b5398d46230
Registration Date
December 29, 2021
Manufacturer
Authorized Representative