Ceruloplasmin - FDA Registration 562d9b00c2feb34303574a214c4ab603
Access comprehensive regulatory information for Ceruloplasmin in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 562d9b00c2feb34303574a214c4ab603 and manufactured by Sentinel CH. SpA.. The device was registered on August 24, 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
562d9b00c2feb34303574a214c4ab603
Ceruloplasmin
FDA ID: 562d9b00c2feb34303574a214c4ab603
Device Classification
Brand Name
Abbott
Registration Information
Analysis ID
562d9b00c2feb34303574a214c4ab603
Registration Date
August 24, 2022
Manufacturer
Authorized Representative

