CEA Rapid Quantitative Test - FDA Registration 08d9c2e1483c4bbc1a88e297bef6587e
Access comprehensive regulatory information for CEA Rapid Quantitative Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 08d9c2e1483c4bbc1a88e297bef6587e and manufactured by Guangzhou Wondfo Biotech Co., Ltd.. The device was registered on August 16, 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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FDA Official Data
08d9c2e1483c4bbc1a88e297bef6587e
CEA Rapid Quantitative Test
FDA ID: 08d9c2e1483c4bbc1a88e297bef6587e
Device Classification
Brand Name
Finecare
Registration Information
Analysis ID
08d9c2e1483c4bbc1a88e297bef6587e
Registration Date
August 16, 2022
Manufacturer
Authorized Representative

