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Knee arthroplasty wedge - UK MHRA Medical Device Registration

Knee arthroplasty wedge is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 209616. The device is manufactured by Zimmer Inc. from United States, classified as General Medical Device.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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MHRA Registered
General Medical Device
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Knee arthroplasty wedge
MHRA Device ID: 209616

Device Type

General Medical Device

Type

Class IIb

Status

DREGIY

Date Registered

Jan 28, 2025

Manufacturer Information

Address

1800 West Center Street

Indiana, Warsaw, United States

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