Midmark Diagnostics Group
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- Devices
- 1
What Midmark Diagnostics Group makes
Midmark Diagnostics Group manufactures the IQMark Vital Signs Monitor, a device designed for continuous monitoring of patient vital signs such as heart rate, respiratory rate, and oxygen saturation. It is intended for use in clinical settings to provide real-time physiological data for patient assessment and care.
The IQMark Vital Signs Monitor is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Midmark Diagnostics Iqmark Vital Signs Monitor Ref K072516
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Midmark Diagnostics Group have in the registry?
The registry currently lists 1 device for Midmark Diagnostics Group. Devices recorded under merged duplicate company entries are counted once.
Which registries list Midmark Diagnostics Group's devices?
Among its 1 most recently registered device, Midmark Diagnostics Group has devices listed in FDA 510(k) (1 device).
What risk classes do Midmark Diagnostics Group's devices fall under?
Among its 1 most recently registered device, the classes recorded for Midmark Diagnostics Group's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Midmark Diagnostics Group in the registry?
The most recently registered devices listed for Midmark Diagnostics Group include MIDMARK DIAGNOSTICS IQMARK VITAL SIGNS MONITOR.