Bone Screw - FDA Registration 37a869f160faeb0a1f960e597bde8bc3
Access comprehensive regulatory information for Bone Screw in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 37a869f160faeb0a1f960e597bde8bc3 and manufactured by WUHAN MINDRAY SCIENTIFIC CO.LTD.. The device was registered on November 18, 2022.
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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FDA Official Data
37a869f160faeb0a1f960e597bde8bc3
Bone Screw
FDA ID: 37a869f160faeb0a1f960e597bde8bc3
Device Classification
Brand Name
Mindray
Registration Information
Analysis ID
37a869f160faeb0a1f960e597bde8bc3
Registration Date
November 18, 2022
Manufacturer
Authorized Representative

