PTFE GUIDEWIRE (PTFE COATED UROLOGICAL GUIDEWIRES), 3 CM FLEXIBLE TIP - FDA Registration MDR-01977

Access comprehensive regulatory information for PTFE GUIDEWIRE (PTFE COATED UROLOGICAL GUIDEWIRES), 3 CM FLEXIBLE TIP in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01977 and manufactured by Boston Scientific Corporation - 300 Boston Scientific Way Marlborough, MA 01752-1234 USA mfd. by: Lake Region Medical Ltd. - Butlersland New Ross Co Wexford, Ireland For Lake Region Medical Ltd.- 340 Lake Hazeltine Drive Chaska, Minnesota 55318 USA in USA. The device was registered on May 20, 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.