Philippines FDA registration MDR-09958C

Weck® Horizon™ Manual Load Ligating Clip Applier, Curved Jaw

Philippines flagPhilippines·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·Ireland·Issued January 17, 2023 – July 08, 2026
Device information
Product Name
Weck® Horizon™ Manual Load Ligating Clip Applier, Curved Jaw
Registration Number
MDR-09958C
Manufacturer details
Country of Origin
Ireland
Importer & distribution
Importer/Distributor
Medicotek, Inc.
Registration dates
Issuance Date
January 17, 2023
Expiry Date
July 08, 2026
About this record

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-09958C 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 January 17, 2023.

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.

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