Myanmar FDA registration 00bb0592dd869ba95c8c31e92402af24
Finecare
Device classification
- Brand Name
- WONDFO
Registration information
- Analysis ID
- 00bb0592dd869ba95c8c31e92402af24
- Registration Date
- September 07, 2022
Manufacturer
Authorized Representative
About this record
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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