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weck Visistat® 35W Disposable Skin Staple, Wide - FDA Registration DVR-4651

Access comprehensive regulatory information for weck Visistat® 35W Disposable Skin Staple, Wide in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-4651 and manufactured by Teleflex Medical IDA Business and Technolgy Park, Dublin Road, Athlone, Co. Westmeath, Ireland Mfd By: Hudson Respiratory Care Tecate S. De R.L. De C.V. A Teleflex Medical Company - Prologacion Misison Eusebio, Kino No. 1316 Rancho El Descaso, Tecate, Baja California, 21478, MExico for TEleflex MEdical - 3015 CArrington Mill BLvd., Morrisville, NC, 27560, USA in Ireland. The device was registered on April 22, 2024.

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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Ireland
DVR-4651
weck Visistat® 35W Disposable Skin Staple, Wide
Registered medical device in Philippines
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Importer & Distribution
Importer/Distributor
Medicotek, Inc.
Registration Dates
Issuance Date
April 22, 2024
Expiry Date
September 13, 2028