FinecareTM cTn I Rapid Quantitative Test - FDA Registration b2ee82ce78c892e5d2cbcd28a726a2b4
Access comprehensive regulatory information for FinecareTM cTn I Rapid Quantitative Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID b2ee82ce78c892e5d2cbcd28a726a2b4 and manufactured by Guangzhou Wondfo Biotech Co., Ltd.. The device was registered on October 15, 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
b2ee82ce78c892e5d2cbcd28a726a2b4
FinecareTM cTn I Rapid Quantitative Test
FDA ID: b2ee82ce78c892e5d2cbcd28a726a2b4
Device Classification
Brand Name
Wondfo
Registration Information
Analysis ID
b2ee82ce78c892e5d2cbcd28a726a2b4
Registration Date
October 15, 2022
Manufacturer
Authorized Representative

