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WECK® HEM-O-LOK® NON-ABSORBALBE POLYMER LIGATING CLIP - FDA Registration DVR-6346

Access comprehensive regulatory information for WECK® HEM-O-LOK® NON-ABSORBALBE POLYMER LIGATING CLIP in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-6346 and manufactured by Teleflex Medical IDA Business and Technology Park, Dublin Road, Athlone, Co. Westmeath, Ireland Mfd By: Hudson Respiratory Care Tecate S. de R.L. de C.V. - A Teleflex Medical Company Prolongacion Mision Eusebio Kino No. 1316 Rancho El Descano, Tecate, BAja California, 21478, Mexico For: Teleflex Medical - 3015 Carrington Mill Blvd. Morrisville, NC 27560, USA in Ireland. The device was registered on March 21, 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-6346
WECK® HEM-O-LOK® NON-ABSORBALBE POLYMER LIGATING CLIP
Registered medical device in Philippines
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Importer & Distribution
Importer/Distributor
Medicotek, Inc.
Registration Dates
Issuance Date
March 21, 2024
Expiry Date
January 10, 2029