Myanmar FDA registration 610d26bfe5a151ca122a291e131c9a17
One Step HBsAg Whole Blood/Serum/Plasma Test
Device classification
- Brand Name
- Wondfo
Registration information
- Analysis ID
- 610d26bfe5a151ca122a291e131c9a17
- Registration Date
- October 14, 2022
Manufacturer
Authorized Representative
About this record
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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