Bedside Clinical Systems, Inc.
Country not established
- Devices
- 1
What Bedside Clinical Systems, Inc. makes
Bedside Clinical Systems, Inc. manufactures the Bedside Paediatric Early Warning System (BedsidePEWS), a monitoring device designed to assess and alert clinicians to deteriorating paediatric patient conditions in real time.
The BedsidePEWS is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) premarket notification process. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bedside Clinical Systems, Inc. have in the registry?
The registry currently lists 1 device for Bedside Clinical Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bedside Clinical Systems, Inc.'s devices?
Among its 1 most recently registered device, Bedside Clinical Systems, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Bedside Clinical Systems, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Bedside Clinical Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bedside Clinical Systems, Inc. in the registry?
The most recently registered devices listed for Bedside Clinical Systems, Inc. include BEDSIDE PAEDIATRIC EARLY WARNING SYSTEM (BEDSIDEPEWS).