Eu Mdd
Eu Md Class 3
On The Market
🇺🇸 United States
RECELL®
Devices (same UDI-DI)
1
Certificates
2
Countries
21
Notified Bodies
2
Basic Information
- Primary DI
- 00851707004118
- Basic UDI-DI Code
- B-00851707004118
- Reference
- C3RL01-B:EU
- Device Types
-
Single use Sterile
- Regulation
- Eu Mdd
- Classification
- Eu Md Class 3
- Status
- On The Market
- Manufacturer
- AVITA Medical Americas, LLC
CND Nomenclature Codes
| Code | Description |
|---|---|
| Z12019003 | WOUND TREATMENT EQUIPMENT |
Certificates
| Type | Number | Notified Body | Status |
|---|---|---|---|
| MDD Annex II Section 4 | US19/819943500 | SGS Belgium NV | Expired |
| MDD Annex II (excluding section 4) | US19/819943480 | SGS Belgium NV | Expired |
Available In Countries
🇦🇹 Austria
🇧🇪 Belgium
🇨🇿 Czechia
🇩🇪 Germany
🇩🇰 Denmark
🇬🇷 Greece
🇪🇸 Spain
🇫🇮 Finland
🇫🇷 France
🇭🇷 Croatia
🇮🇪 Ireland
🇮🇹 Italy
🇱🇺 Luxembourg
🇳🇱 Netherlands
🇳🇴 Norway
🇵🇱 Poland
🇵🇹 Portugal
🇸🇪 Sweden
🇸🇰 Slovakia
🇹🇷 Türkiye
🇬🇧 United Kingdom
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