Pure Global

HIV 1/2 Ab Plus Combo Rapid Test - FDA Registration 6e209fd7b44ac7cd7c4e086a22c2e231

Access comprehensive regulatory information for HIV 1/2 Ab Plus Combo Rapid Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 6e209fd7b44ac7cd7c4e086a22c2e231 and manufactured by CTK Biotech, Inc.. The device was registered on November 09, 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
6e209fd7b44ac7cd7c4e086a22c2e231
HIV 1/2 Ab Plus Combo Rapid Test
FDA ID: 6e209fd7b44ac7cd7c4e086a22c2e231
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Classification
Brand Name
Aria Brand
Registration Information
Analysis ID
6e209fd7b44ac7cd7c4e086a22c2e231
Registration Date
November 09, 2022
Manufacturer
Authorized Representative