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Combi-pack & Kit - FDA Registration 7b1ac2601278d7fd2dd78eef13152d33

Access comprehensive regulatory information for Combi-pack & Kit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 7b1ac2601278d7fd2dd78eef13152d33 and manufactured by Geistlich Pharma AG. The device was registered on August 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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7b1ac2601278d7fd2dd78eef13152d33
Combi-pack & Kit
FDA ID: 7b1ac2601278d7fd2dd78eef13152d33
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Device Classification
Brand Name
Spiritual
Registration Information
Analysis ID
7b1ac2601278d7fd2dd78eef13152d33
Registration Date
August 30, 2022
Manufacturer
Authorized Representative