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ARCHITECT Urine NGAL Assay - FDA Registration e9fa62b36f2dc7f43be997b4dd6652ac

Access comprehensive regulatory information for ARCHITECT Urine NGAL Assay in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID e9fa62b36f2dc7f43be997b4dd6652ac and manufactured by Abbott Ireland Diagnostics Division. The device was registered on February 22, 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
e9fa62b36f2dc7f43be997b4dd6652ac
ARCHITECT Urine NGAL Assay
FDA ID: e9fa62b36f2dc7f43be997b4dd6652ac
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Device Classification
Brand Name
Abbott
Registration Information
Analysis ID
e9fa62b36f2dc7f43be997b4dd6652ac
Registration Date
February 22, 2022
Authorized Representative