Pure Global

Sirolimus-Eluting Coronary Stents (Orsiro) - FDA Registration 9f9edfc8f2d83c2e11481da96e941206

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.

Free Database
Powered by Pure Global AI
FDA Official Data
9f9edfc8f2d83c2e11481da96e941206
Sirolimus-Eluting Coronary Stents (Orsiro)
FDA ID: 9f9edfc8f2d83c2e11481da96e941206
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Classification
Brand Name
BIOTRONIK
Registration Information
Analysis ID
9f9edfc8f2d83c2e11481da96e941206
Registration Date
January 10, 2022
Manufacturer
Authorized Representative