Pure Global AI
Myanmar FDA registration 8096b731e041fdf162d53af7ce2890dc

S. Typhi/Paratyphi Ag Rapid Test

MyanmarOnsiteCTK Biotech. Inc.Registered December 01, 2022
VerifiedFDA Myanmar · official registry
Device classification
Brand Name
Onsite
Registration information
Analysis ID
8096b731e041fdf162d53af7ce2890dc
Registration Date
December 01, 2022
Manufacturer
Authorized Representative
About this record

Access comprehensive regulatory information for S. Typhi/Paratyphi Ag Rapid Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 8096b731e041fdf162d53af7ce2890dc and manufactured by CTK Biotech. Inc.. The device was registered on December 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.