Finecare - FDA Registration 00bb0592dd869ba95c8c31e92402af24
Access comprehensive regulatory information for Finecare in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 00bb0592dd869ba95c8c31e92402af24 and manufactured by Guangzhou Wondfo Biotech Co.,Ltd.. The device was registered on September 07, 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
00bb0592dd869ba95c8c31e92402af24
Finecare
FDA ID: 00bb0592dd869ba95c8c31e92402af24
Device Classification
Brand Name
WONDFO
Registration Information
Analysis ID
00bb0592dd869ba95c8c31e92402af24
Registration Date
September 07, 2022
Manufacturer
Authorized Representative

