TYDAL (Widal Antigens for Slide and Tube Tests) - FDA Registration 0d88c540298f63b3d24e1e03f2f939f6
Access comprehensive regulatory information for TYDAL (Widal Antigens for Slide and Tube Tests) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 0d88c540298f63b3d24e1e03f2f939f6 and manufactured by Tulip Diagnostics (P) Ltd. The device was registered on July 16, 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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FDA Official Data
0d88c540298f63b3d24e1e03f2f939f6
TYDAL (Widal Antigens for Slide and Tube Tests)
FDA ID: 0d88c540298f63b3d24e1e03f2f939f6
Device Classification
Brand Name
Tulip
Registration Information
Analysis ID
0d88c540298f63b3d24e1e03f2f939f6
Registration Date
July 16, 2022
Manufacturer
Authorized Representative

