Devices (same UDI-DI)
110
Certificates
1
Countries
5
Notified Bodies
1
Basic Information
- Primary DI
- 07630033312646
- Basic UDI-DI Code
- 076300333IF_CBLCATHL4
- Reference
- IR30/10
- 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
🇩🇪 Germany
🇪🇸 Spain
🇭🇷 Croatia
🇱🇹 Lithuania
🇱🇻 Latvia
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.
InRo®
Device
EU MDR
·
Eu Md Class 3
·Rontis Corporation SA·On the market·1 country
InRo®
Device
EU MDR
·
Eu Md Class 3
·Rontis Corporation SA·On the market·1 country
InRo®
Device
EU MDR
·
Eu Md Class 3
·Rontis Corporation SA·On the market·1 country
InRo®
Device
EU MDR
·
Eu Md Class 3
·Rontis Corporation SA·On the market·1 country
InRo®
Device
EU MDR
·
Eu Md Class 3
·Rontis Corporation SA·On the market·1 country
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