Rebase II (Normal) (Light Pink)(Chairside Hard Denture Reline Material) - FDA Registration 2ac6fde4b875ddb767199de09c4a72ea
Access comprehensive regulatory information for Rebase II (Normal) (Light Pink)(Chairside Hard Denture Reline Material) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 2ac6fde4b875ddb767199de09c4a72ea and manufactured by Tokuyama Dental Corporation. The device was registered on December 11, 2021.
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
2ac6fde4b875ddb767199de09c4a72ea
Rebase II (Normal) (Light Pink)(Chairside Hard Denture Reline Material)
FDA ID: 2ac6fde4b875ddb767199de09c4a72ea
Device Classification
Brand Name
Tokuyama Dental
Registration Information
Analysis ID
2ac6fde4b875ddb767199de09c4a72ea
Registration Date
December 11, 2021
Manufacturer
Authorized Representative

