One Step MAU Rapid Quantitative Test - FDA Registration db64ff8a7f8a40a8d3708905f00b0062
Access comprehensive regulatory information for One Step MAU Rapid Quantitative Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID db64ff8a7f8a40a8d3708905f00b0062 and manufactured by Guangzhou Wondfo Biotech Co., Ltd.. The device was registered on August 16, 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
db64ff8a7f8a40a8d3708905f00b0062
One Step MAU Rapid Quantitative Test
FDA ID: db64ff8a7f8a40a8d3708905f00b0062
Device Classification
Brand Name
Finecare
Registration Information
Analysis ID
db64ff8a7f8a40a8d3708905f00b0062
Registration Date
August 16, 2022
Manufacturer
Authorized Representative

