Baxter Healthcare Corproration
Country not established
- Devices
- 1
What Baxter Healthcare Corproration makes
Baxter Healthcare Corporation manufactures patient monitoring systems, including the Hillrom Heart and Respiration Rate Monitoring System powered by EarlySense. This device is designed to continuously track heart and respiration rates, providing real-time physiological data for clinical use.
The company’s portfolio is regulated under Class II medical devices in the United States, with relevant products authorised through the FDA’s 510(k) clearance process. The manufacturer is based in the US.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Baxter Healthcare Corproration have in the registry?
The registry currently lists 1 device for Baxter Healthcare Corproration. Devices recorded under merged duplicate company entries are counted once.
Which registries list Baxter Healthcare Corproration's devices?
Among its 1 most recently registered device, Baxter Healthcare Corproration has devices listed in FDA 510(k) (1 device).
What risk classes do Baxter Healthcare Corproration's devices fall under?
Among its 1 most recently registered device, the classes recorded for Baxter Healthcare Corproration's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Baxter Healthcare Corproration in the registry?
The most recently registered devices listed for Baxter Healthcare Corproration include Hillrom Heart and Respiration Rate Monitoring System powered by EarlySense.