Eumedics Medizintechnik Und Marketing GmbH
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- Devices
- 1
What Eumedics Medizintechnik Und Marketing GmbH makes
Eumedics Medizintechnik produces the RespiFit S (model RS-LR1001004), a respiratory device designed for use in medical settings to support ventilation or inhalation therapy.
The company’s portfolio is regulated under FDA’s Class II device category and is listed via the 510(k) premarket notification process. The manufacturer is based in the United States.
Catalogue
Respifit S, Model Rs-LR1001004 Ref K080299
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Eumedics Medizintechnik Und Marketing GmbH have in the registry?
The registry currently lists 1 device for Eumedics Medizintechnik Und Marketing GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eumedics Medizintechnik Und Marketing GmbH's devices?
Among its 1 most recently registered device, Eumedics Medizintechnik Und Marketing GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Eumedics Medizintechnik Und Marketing GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Eumedics Medizintechnik Und Marketing GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Eumedics Medizintechnik Und Marketing GmbH in the registry?
The most recently registered devices listed for Eumedics Medizintechnik Und Marketing GmbH include RESPIFIT S, MODEL RS-LR1001004.