Eu Mdr
Eu Md Class 2a
On The Market
🇺🇸 United States
C2 Cryoablation(TM) System catheter
Devices (same UDI-DI)
7
Certificates
0
Countries
2
Notified Bodies
0
Basic Information
- Primary DI
- 00854924006200
- Basic UDI-DI Code
- 4961333020017XZ
- Reference
- FG-1020
- Device Types
-
Single use Sterile
- Regulation
- Eu Mdr
- Classification
- Eu Md Class 2a
- Status
- On The Market
- Manufacturer
- PENTAX MEDICAL A DIVISION OF PENTAX OF AMERICA INC
Additional Description
The C2 CryoBalloon™ Ablation System is used to ablate unwanted tissue in the gastrointestinal tract, including treatment of Barrett’s oesophagus and squamous dysplasia, by application of extreme cold.
CND Nomenclature Codes
| Code | Description |
|---|---|
| G0301010101 | OESOPHAGEAL BALLOON CATHETERS, LOW PRESSURE |
Available In Countries
🇩🇪 Germany
🇳🇱 Netherlands
Related Devices
The Basic UDI-DI associated with this device has 7 devices in total. Below are some other devices sharing the same Basic UDI-DI.
C2 Cryoablation(TM) System catheter
Device
EU MDR
·
Eu Md Class 2a
·PENTAX MEDICAL A DIVISION OF PENTAX OF AMERICA INC·On the market·2 countries
C2 Cryoablation(TM) System catheter
Device
EU MDR
·
Eu Md Class 2a
·PENTAX MEDICAL A DIVISION OF PENTAX OF AMERICA INC·On the market·2 countries
C2 Cryoablation(TM) System catheter
Device
EU MDR
·
Eu Md Class 2a
·PENTAX MEDICAL A DIVISION OF PENTAX OF AMERICA INC·On the market·2 countries
C2 Cryoablation(TM) System catheter
Device
EU MDR
·
Eu Md Class 2a
·PENTAX MEDICAL A DIVISION OF PENTAX OF AMERICA INC·On the market·2 countries
C2 Cryoablation(TM) System catheter
Device
EU MDR
·
Eu Md Class 2a
·PENTAX MEDICAL A DIVISION OF PENTAX OF AMERICA INC·On the market·2 countries
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