Myanmar FDA registration 2535d82e2100f4ed6a1ed1e2e8f5fbde
Bioline Dengue NS1 Ag
Device classification
- Brand Name
- Bioline
Registration information
- Analysis ID
- 2535d82e2100f4ed6a1ed1e2e8f5fbde
- Registration Date
- March 25, 2022
Manufacturer
Authorized Representative
About this record
Access comprehensive regulatory information for Bioline Dengue NS1 Ag in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 2535d82e2100f4ed6a1ed1e2e8f5fbde and manufactured by Abbott Diagnostics Korea Inc.. The device was registered on March 25, 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.
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