Myanmar FDA registration 066ffc52a848dff7f39a14a74a72c3c4
MaxLINE Syphilis/TP Rapid Test
Device classification
- Brand Name
- MaxLINE
Registration information
- Analysis ID
- 066ffc52a848dff7f39a14a74a72c3c4
- Registration Date
- July 27, 2022
Manufacturer
Authorized Representative
About this record
Access comprehensive regulatory information for MaxLINE Syphilis/TP Rapid Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 066ffc52a848dff7f39a14a74a72c3c4 and manufactured by Avecon Healthcare Pvt. Ltd.. The device was registered on July 27, 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