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Link® T.O.P Polyethylene Insert, Type: Anti-Luxation - Cementless Orthopaedic Implants - Acetabular Cup System For Total Hip Replacement - FDA Registration MDR-05181

Access comprehensive regulatory information for Link® T.O.P Polyethylene Insert, Type: Anti-Luxation - Cementless Orthopaedic Implants - Acetabular Cup System For Total Hip Replacement in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-05181 and manufactured by Waldemar Link GmbH & Co. KG Barkhausenweg 10, 22339 Hamburg, Germany in Germany. The device was registered on January 15, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (Westech Meditrade, 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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Germany
MDR-05181
Link® T.O.P Polyethylene Insert, Type: Anti-Luxation - Cementless Orthopaedic Implants - Acetabular Cup System For Total Hip Replacement
Registered medical device in Philippines
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Device Information
Product Name
Link® T.O.P Polyethylene Insert, Type: Anti-Luxation - Cementless Orthopaedic Implants - Acetabular Cup System For Total Hip Replacement
Registration Number
MDR-05181
Manufacturer Details
Importer & Distribution
Importer/Distributor
Westech Meditrade, Inc.
Registration Dates
Issuance Date
January 15, 2024
Expiry Date
February 13, 2028