Medos Medizintechnik AG
Country not established
- Devices
- 3
What Medos Medizintechnik AG makes
Medos Medizintechnik AG manufactures extracorporeal membrane oxygenation (ECMO) devices, including the MEDOS HILITE 7000, HILITE 7000 LT, and HILITE Infant oxygenators. These products are designed for use in cardiopulmonary bypass and ECMO therapies to support oxygenation and circulation in patients requiring advanced respiratory or cardiac assistance.
The company’s oxygenators are classified as Class II medical devices under FDA regulations and are listed via the 510(k) pathway. These devices are intended for use in the United States, where they are subject to compliance with FDA requirements for extracorporeal blood oxygenation systems.
Catalogue
Medos Hilite 7000 & 7000 Lt Oxygenator Ref K133261
Regimes: 510(k) Registry: 510(k)Medos Hilite Oxygenator Ref K140177
Regimes: 510(k) Registry: 510(k)Medos Hilite Infant Oxygenator Ref K140181
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medos Medizintechnik AG have in the registry?
The registry currently lists 3 devices for Medos Medizintechnik AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medos Medizintechnik AG's devices?
Among its 3 most recently registered devices, Medos Medizintechnik AG has devices listed in FDA 510(k) (3 devices).
What risk classes do Medos Medizintechnik AG's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Medos Medizintechnik AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medos Medizintechnik AG in the registry?
The most recently registered devices listed for Medos Medizintechnik AG include MEDOS HILITE 7000 & 7000 LT OXYGENATOR, MEDOS HILITE OXYGENATOR and MEDOS HILITE INFANT OXYGENATOR.