Eu Mdr
Eu Md Class 2a
On The Market
🇺🇸 United States
POWERFLEX™ PRO Percutaneous Transluminal Angioplasty (PTA) Catheter
Devices (same UDI-DI)
116
Certificates
0
Countries
32
Notified Bodies
0
Basic Information
- Primary DI
- 20705032059814
- Basic UDI-DI Code
- 07050320000000000000024CF
- Reference
- 4400804S
- Device Types
-
Single use Sterile
- Regulation
- Eu Mdr
- Classification
- Eu Md Class 2a
- Status
- On The Market
- Manufacturer
- Cordis US Corporation
CND Nomenclature Codes
| Code | Description |
|---|---|
| C010402020101 | PTA BALLOON DILATATION CATHETERS |
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
Related Devices
The Basic UDI-DI associated with this device has 116 devices in total. Below are some other devices sharing the same Basic UDI-DI.
POWERFLEX™ PRO Percutaneous Transluminal Angioplasty (PTA) Catheter
Device
EU MDR
·
Eu Md Class 2a
·Cordis US Corporation·On the market·32 countries
POWERFLEX™ PRO Percutaneous Transluminal Angioplasty (PTA) Catheter
Device
EU MDR
·
Eu Md Class 2a
·Cordis US Corporation·On the market·32 countries
POWERFLEX™ PRO Percutaneous Transluminal Angioplasty (PTA) Catheter
Device
EU MDR
·
Eu Md Class 2a
·Cordis US Corporation·On the market·32 countries
POWERFLEX™ PRO Percutaneous Transluminal Angioplasty (PTA) Catheter
Device
EU MDR
·
Eu Md Class 2a
·Cordis US Corporation·On the market·32 countries
POWERFLEX™ PRO Percutaneous Transluminal Angioplasty (PTA) Catheter
Device
EU MDR
·
Eu Md Class 2a
·Cordis US Corporation·On the market·32 countries
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