Endo GIA™ Curved Tip Articulating Vascular/Medium Reload with Tri-staple™ Technology - FDA Registration MDR-01602

Access comprehensive regulatory information for Endo GIA™ Curved Tip Articulating Vascular/Medium Reload with Tri-staple™ Technology in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01602 and manufactured by Covidien Private Limited-50 Pasir Panjang Road, #04-51 Mapletree Business City, Singapore Mfd by: Covidien- 60 Middletown Avenue, North Haven CT 06473, USA For: Covidien LLC-15 Hampshire Street Mansfield, MA 02048, USA in USA. The device was registered on May 22, 2025.

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