Myanmar FDA registration 0511f31e643170cda3a82a49f92591c6
SKIN-GRAFT CARRF/BA720R1:6STER
Device classification
- Brand Name
- Aesculap
Registration information
- Analysis ID
- 0511f31e643170cda3a82a49f92591c6
- Registration Date
- November 10, 2022
Manufacturer
- Name
- Aesculap AG
Authorized Representative
About this record
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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