Mindray North America
Country not established
- Devices
- 3
What Mindray North America makes
Mindray North America manufactures patient monitoring devices, including the PASSPORT M Series (models 17M and 12M) and the ACCUTORR 7 vital signs monitor. These systems track physiological parameters such as heart rate, blood pressure, and oxygen saturation for clinical use.
The company’s devices are classified as Class II under FDA regulations and are supported by 510(k) clearance. The portfolio is listed in the FDA’s regulatory database, and the company operates with a US-based presence.
Catalogue
Vital Signs Monitor Ref K132037
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Accutorr 7 Vital Signs Monitor Ref K132038
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mindray North America have in the registry?
The registry currently lists 3 devices for Mindray North America. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mindray North America's devices?
Among its 3 most recently registered devices, Mindray North America has devices listed in FDA 510(k) (3 devices).
What risk classes do Mindray North America's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Mindray North America's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mindray North America in the registry?
The most recently registered devices listed for Mindray North America include VITAL SIGNS MONITOR, PASSPORT M SERIES PATIENT MONITORING (INCLUDING MODELS PASSPORT 17M AND PASSPORT 12M) and ACCUTORR 7 VITAL SIGNS MONITOR.