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FLEXIMA™ BILIARY CATHETER SYSTEM KIT - FDA Registration MDR-06375

Access comprehensive regulatory information for FLEXIMA™ BILIARY CATHETER SYSTEM KIT in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-06375 and manufactured by Boston Scientific Corporation - 300 Boston Scientific Way Marlborough MA 01752 USA mfd. By: Boston Scientific Corporation - 2546 First Street Propark El Coyol, Alajuela, Costa Rica in Costa Rica. The device was registered on May 26, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Boston Scientific Philippines, Inc.), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.

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MDR-06375
FLEXIMA™ BILIARY CATHETER SYSTEM KIT
Registered medical device in Philippines
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Device Information
Product Name
FLEXIMA™ BILIARY CATHETER SYSTEM KIT
Registration Number
MDR-06375
Importer & Distribution
Registration Dates
Issuance Date
May 26, 2025
Expiry Date
January 15, 2029