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One Step HBsAg Whole Blood/Serum/Plasma Test - FDA Registration 610d26bfe5a151ca122a291e131c9a17

Access comprehensive regulatory information for One Step HBsAg Whole Blood/Serum/Plasma Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 610d26bfe5a151ca122a291e131c9a17 and manufactured by Guangzhou Wondfo Biotech Co., Ltd.. The device was registered on October 14, 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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610d26bfe5a151ca122a291e131c9a17
One Step HBsAg Whole Blood/Serum/Plasma Test
FDA ID: 610d26bfe5a151ca122a291e131c9a17
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Device Classification
Brand Name
Wondfo
Registration Information
Analysis ID
610d26bfe5a151ca122a291e131c9a17
Registration Date
October 14, 2022
Authorized Representative