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Ritter GmbH

Germany Last updated 22 Oct 2026

Devices
52
Registries
EUDAMEDFDA
FDA recalls
0

Catalogue52

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FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Ritter Co. US

What Ritter GmbH makes

Ritter GmbH manufactures pipetting tips for laboratory use, including conductive and non-conductive variants in various volumes (50 µL to 1000 µL). Products include standard tips, filter-tipped tips, tray-packaged sets, and specialized configurations like deep-well (DP) and multi-well formats. Some designs incorporate conductive materials for compatibility with electronic pipettes, while others are insulated for non-conductive applications.

The company’s pipetting tips are classified as Class A medical devices under EU regulations and are registered in the EUDAMED database. The portfolio is listed under the Medical Devices Regulation (MDR) framework, ensuring compliance with EU requirements for low-risk devices. The manufacturer is based in Germany.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Information

Address
55, Kaufbeurer Str., Schwabmünchen, Germany
Phone
+49 8232 5003 45
PRRC contact
Judith Kroll
EUDAMED SRN
DE-MF-000036772
FDA FEI number
3001856801