Dengue NS1+IgG/IgM Rapid Test Cassette (WB/S/P) - FDA Registration 155aef6c7708a7da88159672aa681312
Access comprehensive regulatory information for Dengue NS1+IgG/IgM 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 155aef6c7708a7da88159672aa681312 and manufactured by Zhejiang Orient Gene Biotech Co.,Ltd. The device was registered on October 31, 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
155aef6c7708a7da88159672aa681312
Dengue NS1+IgG/IgM Rapid Test Cassette (WB/S/P)
FDA ID: 155aef6c7708a7da88159672aa681312
Device Classification
Brand Name
DIAGNOSTAR
Registration Information
Analysis ID
155aef6c7708a7da88159672aa681312
Registration Date
October 31, 2022
Manufacturer
Authorized Representative

