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Febrile Antigen kit+Controls - FDA Registration 4e70fc1d388e135774e7bdb79d2d4631

Access comprehensive regulatory information for Febrile Antigen kit+Controls in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 4e70fc1d388e135774e7bdb79d2d4631 and manufactured by Lorne Laboratories Ltd. The device was registered on September 24, 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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4e70fc1d388e135774e7bdb79d2d4631
Febrile Antigen kit+Controls
FDA ID: 4e70fc1d388e135774e7bdb79d2d4631
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Device Classification
Brand Name
Lorne
Registration Information
Analysis ID
4e70fc1d388e135774e7bdb79d2d4631
Registration Date
September 24, 2022