Parascreen (Rapid Test for Malaria Pan/Pf (Device)) - FDA Registration 773b2df2fd19bfdf34ad538883ec7c8b
Access comprehensive regulatory information for Parascreen (Rapid Test for Malaria Pan/Pf (Device)) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 773b2df2fd19bfdf34ad538883ec7c8b and manufactured by Zephyr Biomedicals - A Division of Tulip Diagnostics (P) Ltd.. The device was registered on July 06, 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
773b2df2fd19bfdf34ad538883ec7c8b
Parascreen (Rapid Test for Malaria Pan/Pf (Device))
FDA ID: 773b2df2fd19bfdf34ad538883ec7c8b
Device Classification
Brand Name
Zephyr Biomedicals
Registration Information
Analysis ID
773b2df2fd19bfdf34ad538883ec7c8b
Registration Date
July 06, 2022
Manufacturer
Authorized Representative

