HBsAg Rapid Test Cassette (Whole Blood / Serum / Plasma) - FDA Registration ddb85872cc27c1a6d8c64d5adc6e8a07
Access comprehensive regulatory information for HBsAg 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 ddb85872cc27c1a6d8c64d5adc6e8a07 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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ddb85872cc27c1a6d8c64d5adc6e8a07
HBsAg Rapid Test Cassette (Whole Blood / Serum / Plasma)
FDA ID: ddb85872cc27c1a6d8c64d5adc6e8a07
Device Classification
Brand Name
KANGHUA
Registration Information
Analysis ID
ddb85872cc27c1a6d8c64d5adc6e8a07
Registration Date
November 10, 2022
Manufacturer
Authorized Representative

