FDA device listing
C-Arm OEC 9900,GE C-Arm 9900,GE C-Arm OEC 9900 Elite,GE OEC 9900 C-Arm
FDA device listing 1183105265 · Can Technomed Trading LTD.
Key facts
| Proprietary names | C-Arm OEC 9900,GE C-Arm 9900,GE C-Arm OEC 9900 Elite,GE OEC 9900 C-Arm |
|---|---|
| Owner/operator | Can Technomed Trading LTD. |
| Owner/operator number | 10059827 |
| Premarket submissions | K120613 |
| Product codes | JAA, OWB, OXO |
| Device names | JAA - System, X-Ray, Fluoroscopic, Image-Intensified, OWB - Interventional Fluoroscopic X-Ray System, OXO - Image-Intensified Fluoroscopic X-Ray System, Mobile |
| Device class | Class II |
| Classification regulations (21 CFR) | 892.1650 |
| Review panels | Radiology |
| Registered establishments | CAN TECHNOMED TRADING LTD. |
| Establishment registrations | 3015276088 |
| FEI numbers | 3015276088 |
| Establishment operations | Foreign Exporter |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database