Cys C Rapid Quantitative Test - FDA Registration 9f601665523ba804b7bd563412ad80b2
Access comprehensive regulatory information for Cys C Rapid Quantitative Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 9f601665523ba804b7bd563412ad80b2 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
9f601665523ba804b7bd563412ad80b2
Cys C Rapid Quantitative Test
FDA ID: 9f601665523ba804b7bd563412ad80b2
Device Classification
Brand Name
Finecare
Registration Information
Analysis ID
9f601665523ba804b7bd563412ad80b2
Registration Date
August 16, 2022
Manufacturer
Authorized Representative

