Myanmar FDA registration cfdee8a574fa9f2de98ecddc859ed1d9
Universal Light-Cure Composite Restorative Fluoride Containing Nano Hybrid (reliaFIL LC)
Device classification
- Brand Name
- AHL
Registration information
- Analysis ID
- cfdee8a574fa9f2de98ecddc859ed1d9
- Registration Date
- October 03, 2022
Manufacturer
Authorized Representative
About this record
Access comprehensive regulatory information for Universal Light-Cure Composite Restorative Fluoride Containing Nano Hybrid (reliaFIL LC) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID cfdee8a574fa9f2de98ecddc859ed1d9 and manufactured by Advance Healthcare Ltd.. The device was registered on October 03, 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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