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Endotracheal tube - FDA Registration 9feb51b3c53b1c4376f474766236c3eb

Access comprehensive regulatory information for Endotracheal tube in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 9feb51b3c53b1c4376f474766236c3eb and manufactured by Sterimed Surgicals India Pvt. Ltd. The device was registered on March 15, 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
9feb51b3c53b1c4376f474766236c3eb
Endotracheal tube
FDA ID: 9feb51b3c53b1c4376f474766236c3eb
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Device Classification
Brand Name
Sterimed, Endotracheal tube
Registration Information
Analysis ID
9feb51b3c53b1c4376f474766236c3eb
Registration Date
March 15, 2022
Authorized Representative