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Estelite Posterior Syringe (Resin-based Dental Restorative Material) - FDA Registration 909d49ca55098bf8106ad00c0f5d36df

Access comprehensive regulatory information for Estelite Posterior Syringe (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 909d49ca55098bf8106ad00c0f5d36df 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
909d49ca55098bf8106ad00c0f5d36df
Estelite Posterior Syringe (Resin-based Dental Restorative Material)
FDA ID: 909d49ca55098bf8106ad00c0f5d36df
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Device Classification
Brand Name
Tokuyama Dental
Registration Information
Analysis ID
909d49ca55098bf8106ad00c0f5d36df
Registration Date
December 11, 2021
Authorized Representative