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Optical Biopsy Forceps - FDA Registration 3420acaa7cb31622bfa6e05e73691fe0

Access comprehensive regulatory information for Optical Biopsy Forceps in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 3420acaa7cb31622bfa6e05e73691fe0 and manufactured by KARL STORZ SE & Co. KG. The device was registered on October 24, 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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3420acaa7cb31622bfa6e05e73691fe0
Optical Biopsy Forceps
FDA ID: 3420acaa7cb31622bfa6e05e73691fe0
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Device Classification
Brand Name
Karl Storz
Registration Information
Analysis ID
3420acaa7cb31622bfa6e05e73691fe0
Registration Date
October 24, 2022
Manufacturer
Authorized Representative