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

GOLD ORTOPEDİ SANAYİ VE TİCARET LİMİTED ŞİRKETİ

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

Basic Information

Primary DI
D-8680941526108A4
Basic UDI-DI Code
B-8680941526108A4
Reference
70849-00005
Device Types
Single use Sterile
Regulation
Eu Mdd
Classification
Eu Md Class 3
Status
On The Market

Additional Description

It is designed in oval-dome shape. With this feature, it creates equal load tension by providing a fully compatible contact with the femoral component. It has a 3 protruding mechanism that prevents rotation. It 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-16-417
MDD Annex II Section 4 1984-MDD-19-623

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

Similar Devices

Other on-the-market devices with the same classification (Eu Md Class 3) and regulation (EU MDD).

View all