PORTEX® Epidural Minipack System 1 Clear Catheter, Open End - FDA Registration MDR-10128B

Access comprehensive regulatory information for PORTEX® Epidural Minipack System 1 Clear Catheter, Open End in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10128B and manufactured by Smiths Medical International - 1500, Eureka Park, Lower Pemberton, Ashford, Kent, TN25 4BF, UK Mfd. By: Smiths Medical Czech Republic a.s. - Hrance, Czech Republic for: Smiths Medical ASD, Inc. - 6000 Nathan Lane N., Minneapolis, MN, 55442, USA in UK. The device was registered on June 08, 2022.

This page provides complete registration details including manufacturer information, importer/distributor details (Rebmann 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.