Eu Mdr
Eu Md Class 3
On The Market
🇨🇦 Canada
AORTIC OCCLUSION SYSTEMS
Devices (same UDI-DI)
1
Certificates
1
Countries
12
Notified Bodies
1
Let the assistant research this device
The Research Assistant compiles risk class, certificates, notified bodies and related records — and cites every one.
Free to try · every answer cites its records
Basic Information
- Primary DI
- 10628678061054
- Basic UDI-DI Code
- 628678061001HJ
- Reference
- F01P1
- Device Types
-
Single use Sterile
- Regulation
- Eu Mdr
- Classification
- Eu Md Class 3
- Status
- On The Market
- Manufacturer
- Front Line Medical Technologies Inc.
Additional Description
Vorübergehender Verschluss großer Gefäße
CND Nomenclature Codes
| Code | Description |
|---|---|
| C019009 | AORTIC OCCLUSION SYSTEMS |
Certificates
| Type | Number | Notified Body | Status |
|---|---|---|---|
| MDR Technical Documentation | 28620163227 | Intertek Medical Notified Body AB |
Available In Countries
🇦🇹 Austria
🇧🇪 Belgium
🇩🇪 Germany
🇩🇰 Denmark
🇪🇸 Spain
🇫🇷 France
🇮🇹 Italy
🇱🇺 Luxembourg
🇳🇱 Netherlands
🇳🇴 Norway
🇵🇹 Portugal
🇸🇪 Sweden
Similar Devices
Other on-the-market devices with the same classification (Eu Md Class 3) and regulation (EU MDR).
MYOCARDIAL BIOPSY KITS
Device
EU MDR
·
Eu Md Class 3
·Joline GmbH & Co. KG·On the market·3 countries
Prontoderm® balíček
Device
EU MDR
·
Eu Md Class 3
·On the market
Lifecath XS CT PICC Maestro
Device
EU MDR
·
Eu Md Class 3
·On the market
Lifecath XS CT PICC Maestro
Device
EU MDR
·
Eu Md Class 3
·On the market
Lifecath XS CT PICC Maestro
Device
EU MDR
·
Eu Md Class 3
·On the market
Lifecath XS CT PICC Maestro
Device
EU MDR
·
Eu Md Class 3
·On the market