Dentium Implant System ( Magnetic Assay ) - FDA Registration eb7d37bc29821b4277cd74f48cde7671
Access comprehensive regulatory information for Dentium Implant System ( Magnetic Assay ) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID eb7d37bc29821b4277cd74f48cde7671 and manufactured by Dentium Co., Ltd. The device was registered on November 04, 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
eb7d37bc29821b4277cd74f48cde7671
Dentium Implant System ( Magnetic Assay )
FDA ID: eb7d37bc29821b4277cd74f48cde7671
Device Classification
Brand Name
Dentium
Registration Information
Analysis ID
eb7d37bc29821b4277cd74f48cde7671
Registration Date
November 04, 2022
Manufacturer
Name
Dentium Co., LtdAuthorized Representative

