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Ultrasound Doppler System - FDA Registration bcb6536233dd36a7dd97a2aa1ca50754

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 bcb6536233dd36a7dd97a2aa1ca50754 and manufactured by Bistos Co., Ltd.. The device was registered on November 30, 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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bcb6536233dd36a7dd97a2aa1ca50754
Ultrasound Doppler System
FDA ID: bcb6536233dd36a7dd97a2aa1ca50754
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Device Classification
Brand Name
bistos
Registration Information
Analysis ID
bcb6536233dd36a7dd97a2aa1ca50754
Registration Date
November 30, 2022
Manufacturer
Authorized Representative