Latex Foley Catheter - FDA Registration b0a96d49d7cd08b9847de5ff6174ba8e
Access comprehensive regulatory information for Latex Foley Catheter in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID b0a96d49d7cd08b9847de5ff6174ba8e and manufactured by Well Lead Medical Co., Ltd. The device was registered on June 29, 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
b0a96d49d7cd08b9847de5ff6174ba8e
Latex Foley Catheter
FDA ID: b0a96d49d7cd08b9847de5ff6174ba8e
Device Classification
Brand Name
Wellead
Registration Information
Analysis ID
b0a96d49d7cd08b9847de5ff6174ba8e
Registration Date
June 29, 2022
Manufacturer
Authorized Representative

