Eu Mdd Eu Md Class 3 On The Market 🇹🇷 Türkiye

ZİMED MEDİKAL SANAYİ VE TİCARET LİMİTED ŞİRKETİ

Devices (same UDI-DI)
1
Certificates
2
Countries
32
Notified Bodies
2

Basic Information

Primary DI
D-8680941259242AQ
Basic UDI-DI Code
B-8680941259242AQ
Reference
E.7549-0503
Device Types
Single use Sterile
Regulation
Eu Mdd
Classification
Eu Md Class 3
Status
On The Market

Additional Description

It is used as a binder in Total Knee Prosthesis to ensure that patients with suitable body anatomy have a wider range of knee flexion. It has the function of protecting the posterior cruciate ligaments (C-R) or cutting the posterior cruciate ligaments (P-S) and has a hyperflex feature that allows full flexion of 120 °. Hyperflex insert and insert are identical in design. This inner component is produced from Ultra High Molecular Weight Polyethylene (UHMWPE) material.

CND Nomenclature Codes

Code Description
P0909030101 BICOMPARTMENTAL PRIMARY IMPLANT CEMENTED FEMORAL COMPONENTS

Certificates

Type Number
MDD Annex II (excluding section 4) 1984-MDD-11-129
MDD Annex II Section 4 1984-MDD-11-130

Available In Countries

🇦🇹 Austria 🇧🇪 Belgium 🇧🇬 Bulgaria 🇨🇾 Cyprus 🇨🇿 Czechia 🇩🇪 Germany 🇩🇰 Denmark 🇪🇪 Estonia 🇬🇷 Greece 🇪🇸 Spain 🇫🇮 Finland 🇫🇷 France 🇭🇷 Croatia 🇭🇺 Hungary 🇮🇪 Ireland 🇮🇸 Iceland 🇮🇹 Italy 🇱🇮 Liechtenstein 🇱🇹 Lithuania 🇱🇺 Luxembourg 🇱🇻 Latvia 🇲🇹 Malta 🇳🇱 Netherlands 🇳🇴 Norway 🇵🇱 Poland 🇵🇹 Portugal 🇷🇴 Romania 🇸🇪 Sweden 🇸🇮 Slovenia 🇸🇰 Slovakia 🇹🇷 Türkiye 🇬🇧 United Kingdom

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