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Pulse Oximeter - FDA Registration 0cf271baf6942744de1d47030ea83285

Access comprehensive regulatory information for Pulse Oximeter in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 0cf271baf6942744de1d47030ea83285 and manufactured by Bistos Co.,Ltd. The device was registered on June 23, 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
0cf271baf6942744de1d47030ea83285
Pulse Oximeter
FDA ID: 0cf271baf6942744de1d47030ea83285
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Device Classification
Brand Name
Bistos
Registration Information
Analysis ID
0cf271baf6942744de1d47030ea83285
Registration Date
June 23, 2022
Manufacturer
Authorized Representative