Pure Global

HBV Rapid Test Cassette (WB/S/P) - FDA Registration ca46ac7f9293a1154a0157d41b5fd1e4

Access comprehensive regulatory information for HBV Rapid Test Cassette (WB/S/P) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID ca46ac7f9293a1154a0157d41b5fd1e4 and manufactured by Zhejiang Orient Gene Biotech Co.,Ltd. The device was registered on November 01, 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
ca46ac7f9293a1154a0157d41b5fd1e4
HBV Rapid Test Cassette (WB/S/P)
FDA ID: ca46ac7f9293a1154a0157d41b5fd1e4
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Classification
Brand Name
DIAGNOSTAR
Registration Information
Analysis ID
ca46ac7f9293a1154a0157d41b5fd1e4
Registration Date
November 01, 2022
Authorized Representative