Erich Jaeger B.V.
NetherlandsFDA 510(k) applicant, unverified
- Devices
- 3
What Erich Jaeger B.V. makes
Erich Jaeger B.V. manufactures respiratory monitoring devices, including the Oxycon Alpha with optional ECG capabilities and its modified versions, as well as the Oxycon Pro. These products are designed for measuring oxygen consumption, carbon dioxide production, and ventilation parameters in clinical and research settings.
The company’s portfolio is regulated under FDA Class II devices, with products authorised through the 510(k) clearance pathway. These devices are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Oxyconalpha With Option Ecg Ref K984465
510(k) 510(k)Modification To The Oxyconalpha Ref K980094
510(k) 510(k)Oxycon Pro Ref K992214
510(k) 510(k)
Frequently asked questions
How many devices does Erich Jaeger B.V. have in the registry?
The registry currently lists 3 devices for Erich Jaeger B.V.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Erich Jaeger B.V.'s devices?
Among its 3 most recently registered devices, Erich Jaeger B.V. has devices listed in FDA 510(k) (3 devices).
What risk classes do Erich Jaeger B.V.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Erich Jaeger B.V.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Erich Jaeger B.V. in the registry?
The most recently registered devices listed for Erich Jaeger B.V. include OXYCONALPHA WITH OPTION ECG, MODIFICATION TO THE OXYCONALPHA and OXYCON PRO.