HBsAg (HEPA CARD) (Serum/Plasma) - FDA Registration a35a9dd861c7ef8141064b253a973947
Access comprehensive regulatory information for HBsAg (HEPA CARD) (Serum/Plasma) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID a35a9dd861c7ef8141064b253a973947 and manufactured by Reckon Diagnostics Pvt, Ltd.. The device was registered on February 14, 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
a35a9dd861c7ef8141064b253a973947
HBsAg (HEPA CARD) (Serum/Plasma)
FDA ID: a35a9dd861c7ef8141064b253a973947
Device Classification
Brand Name
RECKON
Registration Information
Analysis ID
a35a9dd861c7ef8141064b253a973947
Registration Date
February 14, 2022
Manufacturer
Authorized Representative

