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Universal Light-Cure Composite Restorative Fluoride Containing Nano Hybrid (reliaFIL LC) - FDA Registration cfdee8a574fa9f2de98ecddc859ed1d9

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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cfdee8a574fa9f2de98ecddc859ed1d9
Universal Light-Cure Composite Restorative Fluoride Containing Nano Hybrid (reliaFIL LC)
FDA ID: cfdee8a574fa9f2de98ecddc859ed1d9
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Device Classification
Brand Name
AHL
Registration Information
Analysis ID
cfdee8a574fa9f2de98ecddc859ed1d9
Registration Date
October 03, 2022
Manufacturer
Authorized Representative