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Patient Monitor - FDA Registration 4152c0d65bde85fa24c6210dd1952405

Access comprehensive regulatory information for Patient Monitor in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 4152c0d65bde85fa24c6210dd1952405 and manufactured by Bistos Co., Ltd.. The device was registered on October 27, 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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4152c0d65bde85fa24c6210dd1952405
Patient Monitor
FDA ID: 4152c0d65bde85fa24c6210dd1952405
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Device Classification
Brand Name
Bistos
Registration Information
Analysis ID
4152c0d65bde85fa24c6210dd1952405
Registration Date
October 27, 2021
Manufacturer
Authorized Representative