Sinus Bur Kit - FDA Registration f24df068e27e677cf6afd5a1b762a873
Access comprehensive regulatory information for Sinus Bur Kit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID f24df068e27e677cf6afd5a1b762a873 and manufactured by Dentium Co., Ltd. The device was registered on November 12, 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
f24df068e27e677cf6afd5a1b762a873
Sinus Bur Kit
FDA ID: f24df068e27e677cf6afd5a1b762a873
Device Classification
Brand Name
Dentium
Registration Information
Analysis ID
f24df068e27e677cf6afd5a1b762a873
Registration Date
November 12, 2022
Manufacturer
Name
Dentium Co., LtdAuthorized Representative

