AFIAS Progesterone - FDA Registration c41667e16675c6d2542d7a904855c6f7
Access comprehensive regulatory information for AFIAS Progesterone in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID c41667e16675c6d2542d7a904855c6f7 and manufactured by Boditech Med Inc. The device was registered on June 30, 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
c41667e16675c6d2542d7a904855c6f7
AFIAS Progesterone
FDA ID: c41667e16675c6d2542d7a904855c6f7
Device Classification
Brand Name
AFIAS
Registration Information
Analysis ID
c41667e16675c6d2542d7a904855c6f7
Registration Date
June 30, 2022
Manufacturer
Name
Boditech Med IncAuthorized Representative

