Angled Abutment - FDA Registration 2c3e1d91ed5648d6c3ae6ab5bb62ff1b
Access comprehensive regulatory information for Angled Abutment in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 2c3e1d91ed5648d6c3ae6ab5bb62ff1b and manufactured by Dentium Co., Ltd. The device was registered on May 17, 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
2c3e1d91ed5648d6c3ae6ab5bb62ff1b
Angled Abutment
FDA ID: 2c3e1d91ed5648d6c3ae6ab5bb62ff1b
Device Classification
Brand Name
Dentium
Registration Information
Analysis ID
2c3e1d91ed5648d6c3ae6ab5bb62ff1b
Registration Date
May 17, 2022
Manufacturer
Name
Dentium Co., LtdAuthorized Representative

