Mid-Link Consulting Co, Ltd.
ChinaFDA applicant, unverified
- Devices
- 1
What Mid-Link Consulting Co, Ltd. makes
Mid-Link Consulting Co, Ltd. manufactures the M Series Patient Monitor, a device designed for real-time physiological parameter monitoring in clinical settings, including heart rate, blood pressure, and oxygen saturation.
The M Series Patient Monitor is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
M Series Patient Monitor Ref K131876
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mid-Link Consulting Co, Ltd. have in the registry?
The registry currently lists 1 device for Mid-Link Consulting Co, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mid-Link Consulting Co, Ltd.'s devices?
Among its 1 most recently registered device, Mid-Link Consulting Co, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Mid-Link Consulting Co, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mid-Link Consulting Co, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mid-Link Consulting Co, Ltd. in the registry?
The most recently registered devices listed for Mid-Link Consulting Co, Ltd. include M SERIES PATIENT MONITOR.