Eppendorf AG
GermanyFDA applicant, unverified
- Devices
- 5
What Eppendorf AG makes
Eppendorf AG manufactures the TransferMan 4m Micromanipulator, a precision instrument designed for microinjection and cell manipulation in laboratory research settings. This device is used for controlled delivery of fluids or particles into cells, enabling applications in genetic engineering, developmental biology, and stem cell research.
The TransferMan 4m Micromanipulator is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
TransferMan 4m Micromanipulator Ref K142207
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 315019588
Frequently asked questions
How many devices does Eppendorf AG have in the registry?
The registry currently lists 5 devices for Eppendorf AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eppendorf AG's devices?
Among its 5 most recently registered devices, Eppendorf AG has devices listed in FDA 510(k) (1 device) and FDA GUDID (4 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Eppendorf AG's devices fall under?
Among its 5 most recently registered devices, the classes recorded for Eppendorf AG's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Eppendorf AG in the registry?
The most recently registered devices listed for Eppendorf AG include TransferMan® 4m 5191000023, CellTram® Air 5176000068, CellTram® Oil 5176000076 and CellTram® vario 5176000084.