Myanmar FDA registration fddede10585921ff3461607e23aeb8eeichroma Myoglobin Neo
MyanmarichromaBoditech Med IncRegistered November 10, 2022
VerifiedFDA Myanmar · official registry
Device classification
- Brand Name
- ichroma
Registration information
- Analysis ID
- fddede10585921ff3461607e23aeb8ee
- Registration Date
- November 10, 2022
Manufacturer
- Name
- Boditech Med Inc
Authorized Representative
About this record
Access comprehensive regulatory information for ichroma Myoglobin Neo in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID fddede10585921ff3461607e23aeb8ee and manufactured by Boditech Med Inc. The device was registered on November 10, 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.