Prosthetic Kit - FDA Registration 6a01c37c85e75eac5982ff17f5fdc419
Access comprehensive regulatory information for Prosthetic Kit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 6a01c37c85e75eac5982ff17f5fdc419 and manufactured by Dentium Co., Ltd. The device was registered on December 16, 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
6a01c37c85e75eac5982ff17f5fdc419
Prosthetic Kit
FDA ID: 6a01c37c85e75eac5982ff17f5fdc419
Device Classification
Brand Name
Dentium
Registration Information
Analysis ID
6a01c37c85e75eac5982ff17f5fdc419
Registration Date
December 16, 2022
Manufacturer
Name
Dentium Co., LtdAuthorized Representative

