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SPECTCT System - FDA Registration c1f502baf2b19b9cb1e105ac8f38addf

Access comprehensive regulatory information for SPECTCT System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID c1f502baf2b19b9cb1e105ac8f38addf and manufactured by Siemens Medical Solutions USA, Inc. The device was registered on December 12, 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
c1f502baf2b19b9cb1e105ac8f38addf
SPECTCT System
FDA ID: c1f502baf2b19b9cb1e105ac8f38addf
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Device Classification
Brand Name
Siemens
Registration Information
Analysis ID
c1f502baf2b19b9cb1e105ac8f38addf
Registration Date
December 12, 2022
Authorized Representative