Root Canal Obturation Cement (Zinc Oxide, Barium Sulphate, Thymol Iodide, Magnesium Stearate) - FDA Registration 8cb48a30733b370bcecf2d72f125e7c8
Access comprehensive regulatory information for Root Canal Obturation Cement (Zinc Oxide, Barium Sulphate, Thymol Iodide, Magnesium Stearate) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 8cb48a30733b370bcecf2d72f125e7c8 and manufactured by Prevest DenPro Limited. The device was registered on May 08, 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.
Free Database
Powered by Pure Global AI
FDA Official Data
8cb48a30733b370bcecf2d72f125e7c8
Root Canal Obturation Cement (Zinc Oxide, Barium Sulphate, Thymol Iodide, Magnesium Stearate)
FDA ID: 8cb48a30733b370bcecf2d72f125e7c8
Device Classification
Brand Name
ENDOSEAL
Registration Information
Analysis ID
8cb48a30733b370bcecf2d72f125e7c8
Registration Date
May 08, 2022
Manufacturer
Authorized Representative

