BiClamp® knife 220 - FDA Registration 855f6dceb07d3ff94fa08aa05df9e068
Access comprehensive regulatory information for BiClamp® knife 220 in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 855f6dceb07d3ff94fa08aa05df9e068 and manufactured by Erbe Elektromedizin GmbH. The device was registered on August 08, 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
855f6dceb07d3ff94fa08aa05df9e068
BiClamp® knife 220
FDA ID: 855f6dceb07d3ff94fa08aa05df9e068
Device Classification
Brand Name
Heir
Registration Information
Analysis ID
855f6dceb07d3ff94fa08aa05df9e068
Registration Date
August 08, 2022
Manufacturer
Authorized Representative

