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

BICOMPARTMENTAL PRIMARY IMPLANT CEMENTED FEMORAL COMPONENTS

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

Basic Information

Primary DI
D-86809412602559D
Basic UDI-DI Code
B-86809412602559D
Reference
E.7849-0005
Device Types
Single use Reprocessed Sterile
Regulation
Eu Mdd
Classification
Eu Md Class 3
Status
On The Market

Additional Description

It is designed as an oval-dome. With this feature, it creates equal load tension by providing fully compatible contact with the femoral component. It has a 3-pronged mechanism that prevents rotation. It is produced from a material with Ultra High Molecular Weight Polyethylene (UHMWPE) and manufactured in accordance with ISO 5834-2 standard. The patellar component has a standard thickness of 12 mm and has different diameters of 23, 26, 29, 32, 35 mm.

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

Similar Devices

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

View all