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ARCHITECT Syphilis TP Reagent Kit - FDA Registration 2aefe12428edaad32461953ad54ddcf5

Access comprehensive regulatory information for ARCHITECT Syphilis TP Reagent Kit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 2aefe12428edaad32461953ad54ddcf5 and manufactured by Abbott GmbH. The device was registered on November 03, 2021.

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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2aefe12428edaad32461953ad54ddcf5
ARCHITECT Syphilis TP Reagent Kit
FDA ID: 2aefe12428edaad32461953ad54ddcf5
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Device Classification
Brand Name
Abbott
Registration Information
Analysis ID
2aefe12428edaad32461953ad54ddcf5
Registration Date
November 03, 2021
Manufacturer
Authorized Representative