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Datex Division Instrumentarium Corp.

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Devices
55

What Datex Division Instrumentarium Corp. makes

The company manufactures patient monitoring devices, including anesthesia multigas monitors like the Capnomac II and Capnomac Ultima, as well as specialized monitors for brain activity, airway function, and metabolic parameters such as the DeltaTrac II metabolic monitor and neuromuscular transmission monitor. Additional products include standalone capnometers (e.g., Normocap 200), pressure/temperature modules, and peripheral devices like graphics printers and video displays for clinical data visualization.

These devices are classified under FDA’s Class I and Class II categories, with regulatory clearance obtained through the 510(k) pathway. The company’s products are listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

How many devices does Datex Division Instrumentarium Corp. have in the registry?

The registry currently lists 55 devices for Datex Division Instrumentarium Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Datex Division Instrumentarium Corp.'s devices?

Among its 50 most recently registered devices, Datex Division Instrumentarium Corp. has devices listed in FDA 510(k) (50 devices).

What risk classes do Datex Division Instrumentarium Corp.'s devices fall under?

Among its 50 most recently registered devices, the classes recorded for Datex Division Instrumentarium Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Datex Division Instrumentarium Corp. in the registry?

The most recently registered devices listed for Datex Division Instrumentarium Corp. include DATEX AS/3 PATIENT MONITOR, DUAL CHENNEL BRAIN ACTIVITY MONITOR, PB GRAPHICS PRINTER AND PB VIDEO DISPLAY and CAPNOMAC II(TM) ANESTHESIA MULTIGAS MONITOR.

Generated automatically from registry data and not verified by a human reviewer.