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Arthrex® Implant System, CMC Mini Tightrope®, 1.1 mm - FDA Registration MDR-10049P

Access comprehensive regulatory information for Arthrex® Implant System, CMC Mini Tightrope®, 1.1 mm in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10049P and manufactured by Arthrex, Inc. - 1370 Creekside Boulevard, Naples, Florida 34108-1945, USA in USA. The device was registered on August 22, 2022.

This page provides complete registration details including manufacturer information, importer/distributor details (PacificSurgical 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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USA
MDR-10049P
Arthrex® Implant System, CMC Mini Tightrope®, 1.1 mm
Registered medical device in Philippines
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Device Information
Product Name
Arthrex® Implant System, CMC Mini Tightrope®, 1.1 mm
Registration Number
MDR-10049P
Manufacturer Details
Importer & Distribution
Importer/Distributor
PacificSurgical Inc.
Registration Dates
Issuance Date
August 22, 2022
Expiry Date
July 23, 2026