Hybrid Knife - FDA Registration 90b4bb3f0c144022791681155fe11e1b
Access comprehensive regulatory information for Hybrid Knife in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 90b4bb3f0c144022791681155fe11e1b and manufactured by Erbe Elektromedizin GmbH. The device was registered on June 13, 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
90b4bb3f0c144022791681155fe11e1b
Hybrid Knife
FDA ID: 90b4bb3f0c144022791681155fe11e1b
Device Classification
Brand Name
Heir
Registration Information
Analysis ID
90b4bb3f0c144022791681155fe11e1b
Registration Date
June 13, 2022
Manufacturer
Authorized Representative

