Eu Mdr
Eu Md Class 3
On The Market
🇨🇭 Switzerland
Europa Ultra™
Devices (same UDI-DI)
110
Certificates
1
Countries
16
Notified Bodies
1
Basic Information
- Primary DI
- 07630033300247
- Basic UDI-DI Code
- 076300333EF_CBLCATHGG
- Reference
- EL30/25
- Device Types
-
Single use Sterile Sterilization
- Regulation
- Eu Mdr
- Classification
- Eu Md Class 3
- Status
- On The Market
- Manufacturer
- Rontis Corporation SA
CND Nomenclature Codes
| Code | Description |
|---|---|
| C010401020101 | PTCA BALLOON DILATION CATHETERS |
Certificates
| Type | Number | Notified Body | Status |
|---|---|---|---|
| MDR Technical Documentation | 44912221174 | TÜV NORD CERT GmbH |
Available In Countries
🇧🇬 Bulgaria
🇨🇾 Cyprus
🇨🇿 Czechia
🇩🇪 Germany
🇪🇪 Estonia
🇬🇷 Greece
🇪🇸 Spain
🇭🇷 Croatia
🇮🇪 Ireland
🇮🇸 Iceland
🇮🇹 Italy
🇱🇻 Latvia
🇵🇹 Portugal
🇷🇴 Romania
🇸🇮 Slovenia
🇸🇰 Slovakia
Related Devices
The Basic UDI-DI associated with this device has 110 devices in total. Below are some other devices sharing the same Basic UDI-DI.
Europa Ultra™
Device
EU MDR
·
Eu Md Class 3
·Rontis Corporation SA·On the market·13 countries
Europa Ultra™
Device
EU MDR
·
Eu Md Class 3
·Rontis Corporation SA·On the market·13 countries
Europa Ultra™
Device
EU MDR
·
Eu Md Class 3
·Rontis Corporation SA·On the market·13 countries
Europa Ultra™
Device
EU MDR
·
Eu Md Class 3
·Rontis Corporation SA·On the market·13 countries
Europa Ultra™
Device
EU MDR
·
Eu Md Class 3
·Rontis Corporation SA·On the market·13 countries
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