Pure Global

STANDARD Q Zika/Dengue Fast Trio - FDA Registration 1a722424a7b0abc3c96d0793c47790da

Access comprehensive regulatory information for STANDARD Q Zika/Dengue Fast Trio in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 1a722424a7b0abc3c96d0793c47790da and manufactured by SD Biosensor, Inc.. The device was registered on October 15, 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
1a722424a7b0abc3c96d0793c47790da
STANDARD Q Zika/Dengue Fast Trio
FDA ID: 1a722424a7b0abc3c96d0793c47790da
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Classification
Brand Name
STANDARD Q
Registration Information
Analysis ID
1a722424a7b0abc3c96d0793c47790da
Registration Date
October 15, 2022
Manufacturer
Authorized Representative