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Medonic M51-D Diluent - FDA Registration 27fbbe1b65ce20556ef2e2b24c3b49e3

Access comprehensive regulatory information for Medonic M51-D Diluent in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 27fbbe1b65ce20556ef2e2b24c3b49e3 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
27fbbe1b65ce20556ef2e2b24c3b49e3
Medonic M51-D Diluent
FDA ID: 27fbbe1b65ce20556ef2e2b24c3b49e3
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Device Classification
Brand Name
Medonic
Registration Information
Analysis ID
27fbbe1b65ce20556ef2e2b24c3b49e3
Registration Date
October 08, 2021
Manufacturer
Authorized Representative