Boditech iFOB Neo Control - FDA Registration e379efefa796a1b72bf35f0734af5e08
Access comprehensive regulatory information for Boditech iFOB Neo Control in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID e379efefa796a1b72bf35f0734af5e08 and manufactured by Boditech Med Inc. The device was registered on July 06, 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
e379efefa796a1b72bf35f0734af5e08
Boditech iFOB Neo Control
FDA ID: e379efefa796a1b72bf35f0734af5e08
Device Classification
Brand Name
Boditech
Registration Information
Analysis ID
e379efefa796a1b72bf35f0734af5e08
Registration Date
July 06, 2022
Manufacturer
Name
Boditech Med IncAuthorized Representative

