HCV Rapid Test Cassette (WB/S/P) - FDA Registration 5b4dfe0bc3c93ee37f55a05e7d9ee587
Access comprehensive regulatory information for HCV Rapid Test Cassette (WB/S/P) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 5b4dfe0bc3c93ee37f55a05e7d9ee587 and manufactured by Zhejiang Orient Gene Biotech Co., Ltd. The device was registered on June 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
5b4dfe0bc3c93ee37f55a05e7d9ee587
HCV Rapid Test Cassette (WB/S/P)
FDA ID: 5b4dfe0bc3c93ee37f55a05e7d9ee587
Device Classification
Brand Name
DIAGNOSTAR
Registration Information
Analysis ID
5b4dfe0bc3c93ee37f55a05e7d9ee587
Registration Date
June 15, 2022
Manufacturer
Authorized Representative

