Myanmar FDA registration e379efefa796a1b72bf35f0734af5e08Boditech iFOB Neo Control
MyanmarBoditechBoditech Med IncRegistered July 06, 2022
VerifiedFDA Myanmar · official registry
Device classification
- Brand Name
- Boditech
Registration information
- Analysis ID
- e379efefa796a1b72bf35f0734af5e08
- Registration Date
- July 06, 2022
Manufacturer
- Name
- Boditech Med Inc
Authorized Representative
About this record
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.