Basic UDI-DI
Eu Mdr
Eu Md Class 1
🇺🇸 United States
C2 Cryoballoon (TM) Ablation System Nitroclip
Code: 4961333020019Y5
Devices
1
Certificates
0
Notified Bodies
0
Auth. Representatives
1
Basic Information
- UDI-DI Code
- 4961333020019Y5
- Issuing Agency
- GS1
- Device Model
- FG-1050
- Types
-
Reusable
- Regulation
- Eu Mdr
- Classification
- Eu Md Class 1
- Manufacturer
- PENTAX MEDICAL A DIVISION OF PENTAX OF AMERICA INC
- Last Updated
- October 02, 2024
Certificate Health
No certificates associated with this Basic UDI-DI.
Associated Devices
This Basic UDI-DI is associated with 1 device.
| Name | Status |
|---|---|
| C2 CryoBalloon™ Ablation System Nitroclip | On the market |