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FOLEY BALLOON CATHETER - FDA Registration 20db633fe3203ad7b69a37c811f49153

Access comprehensive regulatory information for FOLEY BALLOON CATHETER in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 20db633fe3203ad7b69a37c811f49153 and manufactured by Sterimed Surgicals India Pvt. Ltd. The device was registered on March 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
20db633fe3203ad7b69a37c811f49153
FOLEY BALLOON CATHETER
FDA ID: 20db633fe3203ad7b69a37c811f49153
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Device Classification
Brand Name
Sterimed, Foley Balloon Catheter (100% Silicone)
Registration Information
Analysis ID
20db633fe3203ad7b69a37c811f49153
Registration Date
March 23, 2022
Authorized Representative