Latex Foley Catheter ( Silicone Coated ) - FDA Registration 8688ad77d2d9e4f001d9bd81e5b5cbe5
Access comprehensive regulatory information for Latex Foley Catheter ( Silicone Coated ) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 8688ad77d2d9e4f001d9bd81e5b5cbe5 and manufactured by Well Lead Medical Co.,Ltd. The device was registered on March 25, 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
8688ad77d2d9e4f001d9bd81e5b5cbe5
Latex Foley Catheter ( Silicone Coated )
FDA ID: 8688ad77d2d9e4f001d9bd81e5b5cbe5
Device Classification
Brand Name
carePLUS Brand
Registration Information
Analysis ID
8688ad77d2d9e4f001d9bd81e5b5cbe5
Registration Date
March 25, 2022
Manufacturer
Authorized Representative

