ARCHITECT c Reagents - FDA Registration 1b7c97dd451628a30894433e6a9f43e9
Access comprehensive regulatory information for ARCHITECT c Reagents in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 1b7c97dd451628a30894433e6a9f43e9 and manufactured by Sekisui Diagnostics P.E.I. Inc.. 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
1b7c97dd451628a30894433e6a9f43e9
ARCHITECT c Reagents
FDA ID: 1b7c97dd451628a30894433e6a9f43e9
Device Classification
Brand Name
Abbott
Registration Information
Analysis ID
1b7c97dd451628a30894433e6a9f43e9
Registration Date
February 14, 2022
Manufacturer
Authorized Representative

