ARCHITECT
MyanmarAbbottFujirebio Diagnostics Inc.,Registered May 26, 2022
VerifiedFDA Myanmar · official registry
Device classification
- Brand Name
- Abbott
Registration information
- Analysis ID
- b5451ea912f6515f1bddbcf28999112f
- Registration Date
- May 26, 2022
Manufacturer
Authorized Representative
About this record
Access comprehensive regulatory information for ARCHITECT in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID b5451ea912f6515f1bddbcf28999112f and manufactured by Fujirebio Diagnostics Inc.,. The device was registered on May 26, 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.