Percutaneous Achilles Repair Forceps

Primary DI

00840277118509

Basic UDI-DI Code

8402771INNOFORCEP01TM

Reference

8235

Device Types

Sterilization

Regulation

Eu Mdr

Classification

Eu Md Class 1

Status

On The Market

Manufacturer

Innomed, Inc.

Designed to help improve accuracy during percutaneous repair of Achilles tendon ruptures. For Limited Open Achilles Tendon Repair. The bump on the lateral side of each loop allows the surgeon to palpate the exact center of the loop, proximal to distal, and drop a needle just below (patient is prone) or anterior to the bump for the starting point, and aim to just below the bump on the opposite side

The Basic UDI-DI associated with this device has 192 devices in total. Below are some other devices sharing the same Basic UDI-DI.

Other on-the-market devices with the same classification (Eu Md Class 1) and regulation (EU MDR).