Pure Global

Aptima HIV-1 Quant Dx Assay - FDA Registration 5079dcaca78d1f246deaae0ab97703f5

Access comprehensive regulatory information for Aptima HIV-1 Quant Dx Assay in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 5079dcaca78d1f246deaae0ab97703f5 and manufactured by Hologic, Inc.. The device was registered on June 28, 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
5079dcaca78d1f246deaae0ab97703f5
Aptima HIV-1 Quant Dx Assay
FDA ID: 5079dcaca78d1f246deaae0ab97703f5
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Classification
Brand Name
HOLOGIC
Registration Information
Analysis ID
5079dcaca78d1f246deaae0ab97703f5
Registration Date
June 28, 2022
Manufacturer
Authorized Representative