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Medonic M51-L2 Bright - FDA Registration 2ea9c7ab84dea55f9ef540c36a27094f

Access comprehensive regulatory information for Medonic M51-L2 Bright in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 2ea9c7ab84dea55f9ef540c36a27094f and manufactured by Boule Medical AB. The device was registered on October 08, 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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FDA Official Data
2ea9c7ab84dea55f9ef540c36a27094f
Medonic M51-L2 Bright
FDA ID: 2ea9c7ab84dea55f9ef540c36a27094f
Local name: Medonic M51-L2 Lyse
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Device Classification
Brand Name
Medonic
Registration Information
Analysis ID
2ea9c7ab84dea55f9ef540c36a27094f
Registration Date
October 08, 2021
Manufacturer
Authorized Representative