Dengue - FDA Registration 51ee84996f9daa47445c181c23a9115d
Access comprehensive regulatory information for Dengue in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 51ee84996f9daa47445c181c23a9115d and manufactured by Lab-Care Diagnostics (India) Pvt. Ltd.. The device was registered on November 21, 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
51ee84996f9daa47445c181c23a9115d
Dengue
FDA ID: 51ee84996f9daa47445c181c23a9115d
Device Classification
Brand Name
SHUBHAM
Registration Information
Analysis ID
51ee84996f9daa47445c181c23a9115d
Registration Date
November 21, 2022
Manufacturer
Authorized Representative

