Commwell Research & Development Ltd.
Country not established
- Devices
- 5
What Commwell Research & Development Ltd. makes
The company manufactures noninterpretive multichannel electrocardiographs, professional multichannel electrocardiographs, and general-purpose multi-parameter bedside monitors. These devices are designed for clinical use to record and display cardiac electrical activity and vital signs at the patient’s bedside.
The portfolio consists of Class II medical devices, all of which are listed in the FDA’s Unique Device Identifier (UDI) database. The company is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Company details
- DUNS number
- 532013976
- [email protected]
- Phone
- +972523603327
Frequently asked questions
How many devices does COMMWELL RESEARCH & DEVELOPMENT LTD. have in the registry?
The registry currently lists 5 devices for COMMWELL RESEARCH & DEVELOPMENT LTD.. Devices recorded under merged duplicate company entries are counted once.
Which registries list COMMWELL RESEARCH & DEVELOPMENT LTD.'s devices?
Among its 5 most recently registered devices, COMMWELL RESEARCH & DEVELOPMENT LTD. has devices listed in FDA GUDID (5 devices).
What risk classes do COMMWELL RESEARCH & DEVELOPMENT LTD.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for COMMWELL RESEARCH & DEVELOPMENT LTD.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from COMMWELL RESEARCH & DEVELOPMENT LTD. in the registry?
The most recently registered devices listed for COMMWELL RESEARCH & DEVELOPMENT LTD. include Commwell ECG Sentinel System, Commwell PhysioGlove ET System, Commwell ES-ECG System and Commwell ECG Mgmt Sys with ECG Analysis.