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-8680941284459BH
Basic UDI-DI Code
B-8680941284459BH
Reference
R.7462-0016
Device Types
Single use Sterile
Regulation
Eu Mdd
Classification
Eu Md Class 3
Status
On The Market

Additional Description

Proximal to gain distal fixation and rotational stability It is designed to bridge the bone defect. a proven sandblasted surface and It has a biocompatible titanium alloy. A tapered, conical implant body and eight The longitudinal canal provides rotational stability and allows for intraoperative anteversion adjustment.allows. It is produced from titanium alloy manufactured in accordance with ASTM F 136.Monoblock revision stem products have different diameters of 10,11,12,13,14,15,16 and 185 One size option is available in mm.

CND Nomenclature Codes

Code Description
P090804030201 REVISION UNCEMENTED FEMORAL STEMS, WITH FIXED NECK

Certificates

Type Number
MDD Annex II Section 4 1984-MDD-21-824
MDD Annex II (excluding section 4) 1984-MDD-11-129

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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