FDA device listing
OR Camera (TruVidia HD, 4K Camera, 4K Refreshing Unit) and accessories [Baxter]
FDA device listing 1146677910 · BAXTER HEALTHCARE CORPORATION
Key facts
| Proprietary names | OR Camera (TruVidia HD, 4K Camera, 4K Refreshing Unit) and accessories [Baxter] |
|---|---|
| Owner/operator | BAXTER HEALTHCARE CORPORATION |
| Owner/operator number | 1417572 |
| Product codes | KQM |
| Device names | KQM - Camera, Surgical And Accessories |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4160 |
| Review panels | General & Plastic Surgery |
| Registered establishments | Baxter Medical Systems GmbH + Co. KG, Hill-Rom Company, Inc. |
| Establishment registrations | 1066635, 9681407, 3007143268 |
| FEI numbers | 1000182014, 3003184737, 3007143268 |
| Establishment operations | Complaint File Establishment, Manufacturer, Repackager/Relabeler, Specification Developer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed 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