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Ultrasound Doppler System - FDA Registration d262d60efdb806777219099335d1a519

Access comprehensive regulatory information for Ultrasound Doppler System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID d262d60efdb806777219099335d1a519 and manufactured by Bistos Co.,ltd.,Korea. The device was registered on October 30, 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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d262d60efdb806777219099335d1a519
Ultrasound Doppler System
FDA ID: d262d60efdb806777219099335d1a519
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Device Classification
Brand Name
Bistos Brand
Registration Information
Analysis ID
d262d60efdb806777219099335d1a519
Registration Date
October 30, 2021
Manufacturer
Authorized Representative