Carematix Inc.
Country not established FDA establishment FEI 3003982635
- Devices
- 7
- Registrations
- FDA
- FDA recalls
- 0
What Carematix Inc. makes
Carematix Inc. manufactures portable automatic-inflation electronic sphygmomanometers designed for arm or wrist use, intended for blood pressure measurement.
The company’s devices are classified as Class II under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.
Catalogue
- GUDID
- GUDID
Modification To Carematix Wellness System Ref K040966
510(k) 510(k)Carematix Wellness System, Model Cws-5000.1-B Ref K100508
510(k) 510(k)Blip Model Bp-700WF Ref K123020
510(k) 510(k)Carematix Wellness System, Model Cws-5000.1-B Ref K073038
510(k) 510(k)Carematix Wellness System Ref K031840
510(k) 510(k)
Company details
- FDA FEI number
- 3003982635
- Address
- 1 N LaSalle St Suite 4400, CHICAGO, IL, 60602
Frequently asked questions
How many devices does CAREMATIX INC. have in the registry?
The registry currently lists 7 devices for CAREMATIX INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list CAREMATIX INC.'s devices?
Among its 7 most recently registered devices, CAREMATIX INC. has devices listed in FDA 510(k) (5 devices) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do CAREMATIX INC.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for CAREMATIX INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from CAREMATIX INC. in the registry?
The most recently registered devices listed for CAREMATIX INC. include Blipcare BP800, Blipcare BP-700WF, MODIFICATION TO CAREMATIX WELLNESS SYSTEM and CAREMATIX WELLNESS SYSTEM, MODEL CWS-5000.1-B.