Myanmar FDA registration 4b331f374b13df35936cc1f2b4af240a
H. Pylori Ab Combo Rapid Test
Device classification
- Brand Name
- Aria Brand
Registration information
- Analysis ID
- 4b331f374b13df35936cc1f2b4af240a
- Registration Date
- February 26, 2022
Manufacturer
Authorized Representative
About this record
Access comprehensive regulatory information for H. Pylori Ab Combo Rapid Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 4b331f374b13df35936cc1f2b4af240a and manufactured by CTK Biotech, Inc.. The device was registered on February 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.
Free DatabasePowered by Pure Global AIFDA Official Data