Myanmar FDA registration 31ab1bb641d22b3dc4fcbc6253946685
Xpert Xpress SARS-CoV-2
Device classification
- Brand Name
- Cepheid
Registration information
- Analysis ID
- 31ab1bb641d22b3dc4fcbc6253946685
- Registration Date
- April 01, 2022
Manufacturer
- Name
- Cepheid
Authorized Representative
About this record
Access comprehensive regulatory information for Xpert Xpress SARS-CoV-2 in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 31ab1bb641d22b3dc4fcbc6253946685 and manufactured by Cepheid. The device was registered on April 01, 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