Ritter GmbH
Germany DE-MF-000036772 Last updated 22 Oct 2026
- Devices
- 52
- Registries
- EUDAMEDFDA
- FDA recalls
- 0
Catalogue
1000 µl TYPE HT2 with filter Ref 49045-0002
Conductive tips T 350 µL C-tray stacked Ref 49024-0008
300 µl, TYPE HT2 with filter Ref 49045-0001
Non-conductive tips T 200µL Ref 49102-0006
Conductive tips H 1000 µL Ref 49009-0005
Conductive tips HT2 1000 µL filter Ref 49009-0115
Conductive tips T 50 µL filter Ref 49026-0106
Conductive tips T 1000 µL C-tray Ref 49003-0007
Non-conductive tips 1000µL Ref 49103-0006
Conductive tips ST 1100 µL DP Ref 49001-0000
Conductive tips T 1000 µL C-tray filter Ref 49003-0117
Conductive tips R 1000µL filter Ref 49209-0105
blackknights, 1000µl, tray, DP 96 pieces in a tray Ref 49027-0005
Conductive tips T 200 µL DP Ref 49002-0000
Conductive tips T 200 µL Ref 49002-0006
Conductive tips T 50 µL Ref 49026-0006
Blackknights H 1000µl with Filters 8 x 480 Tips Ref 49027-0011
Conductive tips ST 1100 µL filter Ref 49001-0106
Conductive tips T 1000 µL C-tray Ref 49003-0017
Non-conductive tips T 1000µL DP Ref 49103-0000
Non-conductive tips T 200µL DP Ref 49102-0000
Conductive tips QG 50 µL filter Ref 49018-0106
Conductive tips H 50 µL Ref 49010-0003
Conductive tips H 50 µL filter Ref 49010-0105
Conductive tips T 200 µL filter Ref 49002-0106
Conductive tips H 300 µL filter Ref 49008-0105
Conductive tips T 1000 µL DP Ref 49003-0000
Conductive tips T 1000 µL WB filter Ref 49033-0106
Conductive tips T 1000 µL filter Ref 49003-0106
Conductive tips H 300 µL Ref 49008-0003
Non-conductive tips T 1000 µL WB filter Ref 49133-0106
Conductive tips HT2 300 µL Ref 49008-0015
Conductive tips HT2 1000 µL Ref 49009-0015
Conductive tips T 1000 µL WB DP Ref 49033-0000
Conductive tips T 50 µL C-tray filter Ref 49026-0117
Conductive tips H 1000 µL filter Ref 49009-0105
Conductive tips T 50 µL DP Ref 49006-0000
DSX/DS2, 108 sample tips, Ref 49136-0000
Conductive tips HT2 50 µL filter Ref 49010-0115
Non-conductive tips 50µL DP Ref 49106-0000
Conductive tips T 50 µL filter C-Tray Ref 49026-0107
blackknights, 200µl, tray, DP 96 pieces in a tray Ref 49027-0007
Conductive tips HT2 300 µL filter Ref 49008-0115
Conductive tips T 50 µL C-tray Ref 49026-0017
DSX/DS2, 108 reagent tips Ref 49137-0000
conductive tips, 50µl, tray, DP Ref 49026-0000
Conductive tips T 200 µL C-tray Ref 49002-0107
Conductive tips HT2 50 µL Ref 49010-0015
Conductive tips T 1000 µL WB Ref 49033-0006
Showing 1-50 of 52
FDA establishments
- 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.
Frequently asked questions
What types of medical devices does Ritter GmbH manufacture?
Ritter GmbH specializes in manufacturing pipetting tips for laboratory use. These include both conductive and non-conductive variants, available in volumes ranging from 50 µL to 1000 µL. Their product line covers standard tips, filter-tipped tips, tray-packaged sets, and specialized formats like deep-well (DP) and multi-well configurations. Conductive tips are designed for compatibility with electronic pipettes, while non-conductive tips are insulated for safety in non-electronic applications.
Where is Ritter GmbH based, and what does this mean for its regulatory compliance?
Ritter GmbH is based in Germany, which places its devices under the jurisdiction of the European Union’s Medical Devices Regulation (MDR). Since the company’s pipetting tips fall under Class A—considered low-risk—they must still comply with MDR requirements, including registration in the EUDAMED database. This ensures transparency and traceability of the devices within the EU market.
Which regulatory registries list Ritter GmbH’s devices, and why is this important?
Ritter GmbH’s devices are listed in the EUDAMED database, which is the official EU registry for medical devices. This listing is critical because it confirms the manufacturer’s compliance with EU regulatory requirements, including device classification (Class A) and adherence to the Medical Devices Regulation (MDR). It also allows healthcare professionals, regulators, and authorities to verify the legitimacy and traceability of the products.
How are Ritter GmbH’s pipetting tips classified under EU regulations, and what does this classification imply?
Ritter GmbH’s pipetting tips are classified as Class A medical devices under EU regulations. This classification is assigned based on risk assessment criteria, where Class A devices are considered the lowest risk due to their minimal or no significant impact on patient safety or health. While this classification simplifies regulatory requirements, it still requires compliance with MDR provisions, including proper labeling, manufacturing controls, and registration in EUDAMED to ensure market access.
Information
- Country
- Germany
- Address
- 55, Kaufbeurer Str., Schwabmünchen, Germany
- Website
- www.ritter-medical.de
- [email protected]
- Phone
- +49 8232 5003 45
- PRRC contact
- Judith Kroll
- EUDAMED SRN
- DE-MF-000036772
- FDA FEI number
- 3001856801