Cobe Laboratories, Inc.
United StatesFDA applicant, unverified
- Devices
- 77
What Cobe Laboratories, Inc. makes
Cobe Laboratories, Inc. manufactures medical devices for blood processing, dialysis, and critical care, including blood component separators, ultrafiltration control kits, and emergency power sources. Their portfolio includes gas flowmeters for respiratory support, dialysis control units, and mobile consoles for pump systems. Additional products cover cardiotomy reservoir filters, ICU conversion kits, and specialized dialyzers for hemodialysis.
The company’s devices are classified under FDA categories Class I, Class II, and Unclassified (U), with regulatory submissions recorded in the 510(k) database. Their products are listed in the United States, where they comply with applicable FDA requirements for medical devices.
Catalogue
Search and filter all 77 devicesShowing 1-50 of 77
Frequently asked questions
How many devices does Cobe Laboratories, Inc. have in the registry?
The registry currently lists 77 devices for Cobe Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cobe Laboratories, Inc.'s devices?
Among its 50 most recently registered devices, Cobe Laboratories, Inc. has devices listed in FDA 510(k) (50 devices).
What risk classes do Cobe Laboratories, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Cobe Laboratories, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cobe Laboratories, Inc. in the registry?
The most recently registered devices listed for Cobe Laboratories, Inc. include FLOWMETER, OPTIFLO GAS, COBE PPD 1.9, COBE SPECTRA BLOOD COMPONENT SEPARATOR THERAPEUTIC and COBE EMERGENCY POWER SOURCE 43610-000.