Eu Mdd
Eu Md Class 2b
On The Market
🇹🇷 Türkiye
Ortimplant
Devices (same UDI-DI)
1
Certificates
1
Countries
32
Notified Bodies
1
Basic Information
- Primary DI
- 08680941152130
- Basic UDI-DI Code
- B-08680941152130
- Reference
- O6049070
- Device Types
-
Single use Sterilization
- Regulation
- Eu Mdd
- Classification
- Eu Md Class 2b
- Status
- On The Market
Additional Description
It is used for temporary fixation in the treatment of large size fragments (intercondylar femur fractures, femoral neck fractures, femoral head epiphysiolysis, tibial plateau fractures) and ankle arthrodesis and iliosacral dislocations.
CND Nomenclature Codes
| Code | Description |
|---|---|
| P09120603 | CANNULATED SCREWS |
Certificates
| Type | Number | Notified Body | Status |
|---|---|---|---|
| MDD Annex II (excluding section 4) | n.0068/QCO-DM/157-2020 | HTCert (Health Technology Certification Ltd) | Expired |
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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