FLUORIDE RELEASING DENTAL RESTORATIVE MATERIAL (BEAUTIFIL II) (GIOMER) - FDA Registration 60ba72744e46cfc15bc79bb77a1aaf40
Access comprehensive regulatory information for FLUORIDE RELEASING DENTAL RESTORATIVE MATERIAL (BEAUTIFIL II) (GIOMER) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 60ba72744e46cfc15bc79bb77a1aaf40 and manufactured by SHOFU INC.,JAPAN. The device was registered on January 08, 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
60ba72744e46cfc15bc79bb77a1aaf40
FLUORIDE RELEASING DENTAL RESTORATIVE MATERIAL (BEAUTIFIL II) (GIOMER)
FDA ID: 60ba72744e46cfc15bc79bb77a1aaf40
Device Classification
Brand Name
SHOFU BRAND
Registration Information
Analysis ID
60ba72744e46cfc15bc79bb77a1aaf40
Registration Date
January 08, 2022
Manufacturer
Name
SHOFU INC.,JAPANAuthorized Representative

