Eu Mdd
Eu Md Class 3
On The Market
🇺🇸 United States
BioBridge ® Collagen Matrix
Devices (same UDI-DI)
1
Certificates
2
Countries
22
Notified Bodies
2
Basic Information
- Primary DI
- +B218PRT00700M
- Basic UDI-DI Code
- B-+B218PRT00700M
- Reference
- PRT0070
- Device Types
-
Single use Sterile
- Regulation
- Eu Mdd
- Classification
- Eu Md Class 3
- Status
- On The Market
- Manufacturer
- Fibralign Corporation
Additional Description
The Fibralign BioBridge® Collagen Matrix is a sterile, thin collagen ribbon made of highly purified pepsin treated Type 1 porcine collagen and features Fibralign’s Nanoweave® technology.
CND Nomenclature Codes
| Code | Description |
|---|---|
| P900299 | SURGICAL MESHES - OTHER |
Certificates
| Type | Number | Notified Body | Status |
|---|---|---|---|
| MDD Annex II Section 4 | 3821521DE | DEKRA Certification B.V. | Expired |
| MDD Annex II (excluding section 4) | 3821521CE | DEKRA Certification B.V. | Expired |
Available In Countries
🇦🇹 Austria
🇧🇪 Belgium
🇨🇾 Cyprus
🇩🇪 Germany
🇩🇰 Denmark
🇬🇷 Greece
🇪🇸 Spain
🇫🇮 Finland
🇫🇷 France
🇭🇺 Hungary
🇮🇪 Ireland
🇮🇹 Italy
🇱🇮 Liechtenstein
🇱🇺 Luxembourg
🇲🇹 Malta
🇳🇱 Netherlands
🇳🇴 Norway
🇵🇱 Poland
🇷🇴 Romania
🇸🇪 Sweden
🇸🇮 Slovenia
🇬🇧 United Kingdom
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