Orthophos E ( OP E ) ( D3352 ) - FDA Registration 830d67b2db71d10b15d743bdb7456972
Access comprehensive regulatory information for Orthophos E ( OP E ) ( D3352 ) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 830d67b2db71d10b15d743bdb7456972 and manufactured by Sirona Dental Systems GmbH. The device was registered on May 30, 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
830d67b2db71d10b15d743bdb7456972
Orthophos E ( OP E ) ( D3352 )
FDA ID: 830d67b2db71d10b15d743bdb7456972
Device Classification
Brand Name
Dentsply Sirona
Registration Information
Analysis ID
830d67b2db71d10b15d743bdb7456972
Registration Date
May 30, 2022
Manufacturer
Authorized Representative

