Fresenius Kabi Deutschland GmbH
GermanyFDA applicant, unverified FDA FEI 3000147578
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Fresenius Kabi Deutschland GmbH makes
Fresenius Kabi Deutschland GmbH manufactures enteral feeding pumps and associated administration sets designed for continuous or intermittent delivery of nutritional solutions via enteral routes.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3000147578
- Address
- 5 ROBERT-KOCH-STRASSE, BAD HERSFELD Hesse
Frequently asked questions
How many devices does Fresenius Kabi Deutschland GmbH have in the registry?
The registry currently lists 1 device for Fresenius Kabi Deutschland GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fresenius Kabi Deutschland GmbH's devices?
Among its 1 most recently registered device, Fresenius Kabi Deutschland GmbH has devices listed in FDA 510(k) (1 device).
What risk classes do Fresenius Kabi Deutschland GmbH's devices fall under?
Among its 1 most recently registered device, the classes recorded for Fresenius Kabi Deutschland GmbH's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fresenius Kabi Deutschland GmbH in the registry?
The most recently registered devices listed for Fresenius Kabi Deutschland GmbH include COMPAT GO ENTERAL FEEDING PUMP AND ADMINISTRATION SETS.