Dengue IgG/IgM & NS1 Rapid Test Kit (Colloidal Gold) - FDA Registration efd6fea29833e9040dd4e3c9bd1b45d8
Access comprehensive regulatory information for Dengue IgG/IgM & NS1 Rapid Test Kit (Colloidal Gold) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID efd6fea29833e9040dd4e3c9bd1b45d8 and manufactured by Nantong Diagnos Biotechnology Co., Ltd. The device was registered on November 18, 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
efd6fea29833e9040dd4e3c9bd1b45d8
Dengue IgG/IgM & NS1 Rapid Test Kit (Colloidal Gold)
FDA ID: efd6fea29833e9040dd4e3c9bd1b45d8
Device Classification
Brand Name
DIAGNOSIS
Registration Information
Analysis ID
efd6fea29833e9040dd4e3c9bd1b45d8
Registration Date
November 18, 2022
Manufacturer
Authorized Representative

