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SKIN-GRAFT CARRF/BA720R1:6STER - FDA Registration 0511f31e643170cda3a82a49f92591c6

Access comprehensive regulatory information for SKIN-GRAFT CARRF/BA720R1:6STER in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 0511f31e643170cda3a82a49f92591c6 and manufactured by Aesculap AG. The device was registered on November 10, 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
0511f31e643170cda3a82a49f92591c6
SKIN-GRAFT CARRF/BA720R1:6STER
FDA ID: 0511f31e643170cda3a82a49f92591c6
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Device Classification
Brand Name
Aesculap
Registration Information
Analysis ID
0511f31e643170cda3a82a49f92591c6
Registration Date
November 10, 2022
Manufacturer
Authorized Representative