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Palfique Universal FLow (High L, Superlow L, Medium L and Medium), Resin-Based Dental Restorative Material - FDA Registration fe8dad61bb07f493d5f61f61575a96ee

Access comprehensive regulatory information for Palfique Universal FLow (High L, Superlow L, Medium L and Medium), Resin-Based Dental Restorative Material in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID fe8dad61bb07f493d5f61f61575a96ee and manufactured by Tokuyama Dental Corporation. The device was registered on November 01, 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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fe8dad61bb07f493d5f61f61575a96ee
Palfique Universal FLow (High L, Superlow L, Medium L and Medium), Resin-Based Dental Restorative Material
FDA ID: fe8dad61bb07f493d5f61f61575a96ee
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Device Classification
Brand Name
Tokuyama Dental
Registration Information
Analysis ID
fe8dad61bb07f493d5f61f61575a96ee
Registration Date
November 01, 2021
Authorized Representative