Rapid HCV TM - FDA Registration 8d8f417957bbe19ef78fb8bff5effaec
Access comprehensive regulatory information for Rapid HCV TM in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 8d8f417957bbe19ef78fb8bff5effaec and manufactured by Biolab Diagnostics (I) Pvt. 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
8d8f417957bbe19ef78fb8bff5effaec
Rapid HCV TM
FDA ID: 8d8f417957bbe19ef78fb8bff5effaec
Device Classification
Brand Name
Biolab Diagnostics
Registration Information
Analysis ID
8d8f417957bbe19ef78fb8bff5effaec
Registration Date
November 10, 2022
Manufacturer
Authorized Representative

