ASAHI Hyperion Coronary Guide Catheter - FDA Registration 1987026f8deb77b0557549fad9cccedf
Access comprehensive regulatory information for ASAHI Hyperion Coronary Guide Catheter in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 1987026f8deb77b0557549fad9cccedf and manufactured by ASAHI INTECC (THAILAND) CO.,LTD. The device was registered on July 27, 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
1987026f8deb77b0557549fad9cccedf
ASAHI Hyperion Coronary Guide Catheter
FDA ID: 1987026f8deb77b0557549fad9cccedf
Device Classification
Brand Name
ASAHI INTECC
Registration Information
Analysis ID
1987026f8deb77b0557549fad9cccedf
Registration Date
July 27, 2022
Manufacturer
Authorized Representative

