Weck® Horizon™ Manual-Load Ligating Clip Applier, Curved Jaw - FDA Registration MDR-09958A

Access comprehensive regulatory information for Weck® Horizon™ Manual-Load Ligating Clip Applier, Curved Jaw in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-09958A and manufactured by Teleflex Medical IDA Business & Technology Park, Dublin Road, Athlone County, Westmeath, Ireland Mfd. By: Tecomet Inc. 5307 95th Avenue Kenosha Wisconsin 53144 USA For: Teleflex Medical - NC, USA in Ireland. The device was registered on December 02, 2022.

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