DENGUE ANTIGEN NS1 CARD (Whole Blood/Serum/Plasma) - FDA Registration b449f7134508b7559f5c10864a6a219d
Access comprehensive regulatory information for DENGUE ANTIGEN NS1 CARD (Whole Blood/Serum/Plasma) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID b449f7134508b7559f5c10864a6a219d and manufactured by Reckon Diagnostics Pvt, Ltd.. The device was registered on February 16, 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
b449f7134508b7559f5c10864a6a219d
DENGUE ANTIGEN NS1 CARD (Whole Blood/Serum/Plasma)
FDA ID: b449f7134508b7559f5c10864a6a219d
Device Classification
Brand Name
RECKON
Registration Information
Analysis ID
b449f7134508b7559f5c10864a6a219d
Registration Date
February 16, 2022
Manufacturer
Authorized Representative

