HCV Rapid Test Cassette (Whole Blood / Serum / Plasma) - FDA Registration 361349fbfe2c6e168241fd617afb3c1e
Access comprehensive regulatory information for HCV Rapid Test Cassette (Whole Blood / Serum / Plasma) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 361349fbfe2c6e168241fd617afb3c1e and manufactured by Qingdao Hightop Biotech Co.,Ltd. The device was registered on November 10, 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
361349fbfe2c6e168241fd617afb3c1e
HCV Rapid Test Cassette (Whole Blood / Serum / Plasma)
FDA ID: 361349fbfe2c6e168241fd617afb3c1e
Device Classification
Brand Name
KANGHUA
Registration Information
Analysis ID
361349fbfe2c6e168241fd617afb3c1e
Registration Date
November 10, 2022
Manufacturer
Authorized Representative

