Myanmar FDA registration 855f6dceb07d3ff94fa08aa05df9e068

BiClamp® knife 220

Myanmar·Heir·Erbe Elektromedizin GmbH·Registered August 08, 2022

Device classification

Brand Name: Heir

Registration information

Analysis ID: 855f6dceb07d3ff94fa08aa05df9e068
Registration Date: August 08, 2022

Manufacturer

Name: Erbe Elektromedizin GmbH

Authorized Representative

Name: SEA LION COMPANY LIMITED

About this record

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.