Basic UDI-DI
Eu Mdr
Eu Md Class 2a
🇺🇸 United States
Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter - POWERFLEX™ PRO
Code: 07050320000000000000024CF
Devices
116
Certificates
0
Notified Bodies
0
Auth. Representatives
1
Basic Information
- UDI-DI Code
- 07050320000000000000024CF
- Issuing Agency
- GS1
- Types
- None provided
- Regulation
- Eu Mdr
- Classification
- Eu Md Class 2a
- Manufacturer
- Cordis US Corporation
- Last Updated
- October 05, 2023
Certificate Health
No certificates associated with this Basic UDI-DI.
Associated Devices
This Basic UDI-DI is associated with 116 devices.