Myanmar FDA registration 9f9edfc8f2d83c2e11481da96e941206
Sirolimus-Eluting Coronary Stents (Orsiro)
Device classification
- Brand Name
- BIOTRONIK
Registration information
- Analysis ID
- 9f9edfc8f2d83c2e11481da96e941206
- Registration Date
- January 10, 2022
Manufacturer
- Name
- BIOTRONIK AG
Authorized Representative
About this record
Access comprehensive regulatory information for Sirolimus-Eluting Coronary Stents (Orsiro) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 9f9edfc8f2d83c2e11481da96e941206 and manufactured by BIOTRONIK AG. The device was registered on January 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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