Myanmar FDA registration 6ab3bc3af82fe1646bb0b959122129ed
Dual Curing Resin Based Luting Cement
Device classification
- Brand Name
- FUSION ULTRA D/C
Registration information
- Analysis ID
- 6ab3bc3af82fe1646bb0b959122129ed
- Registration Date
- May 14, 2022
Manufacturer
Authorized Representative
About this record
Access comprehensive regulatory information for Dual Curing Resin Based Luting Cement in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 6ab3bc3af82fe1646bb0b959122129ed and manufactured by Prevest DenPro Limited. The device was registered on May 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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