Geuder AG
Active in EUDAMEDGermanyfrom SRN EUDAMED FDA SRN DE-MF-000008044 FEI 3003408840
- Devices
- 7
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
EU certificates
1 of 1 in force.
Market reach
- European Union
- EUDAMED actor, 1 certificate
- United States
- FDA establishment
What Geuder AG makes
Geuder AG manufactures ophthalmic irrigation/infusion/aspiration cannulas, specifically the Saad Unfolding Cannula with 1 front and 4 side ports, 27g/0.4mm, which are designed for single-use in ophthalmic procedures.
The company's products are classified as Class IIa medical devices and are listed in the EUDAMED regulatory registry. Geuder AG is based in Germany.
Catalogue
VIVOS device system Ref G-90001
Regimes: CE MDR Registry: EUDAMEDVIVOS device system Ref G-90002
Regimes: CE MDR Registry: EUDAMEDMulti-Patient Cassette VIVOS Ref G-90010
Regimes: CE MDR Registry: EUDAMEDFootswitch VIVOS Ref G-90030
Regimes: CE MDR Registry: EUDAMEDVIVOS device system Ref G-90003
Regimes: CE MDR Registry: EUDAMEDSingle-Patient Cassette VIVOS Ref G-90011
Regimes: CE MDR Registry: EUDAMED- Regimes: CE MDD Registry: EUDAMED
Company details
- EUDAMED SRN
- DE-MF-000008044
- FDA FEI number
- 3003408840
- EU VAT number
- DE 143459517
- EUDAMED status
- Active
- EUDAMED registered name
- Geuder AG
- EUDAMED abbreviated name
- Geuder AG
- Registered address
- 4, Hertzstraße, 69126, Heidelberg, Germany
- Website
- www.geuder.de
- [email protected]
- Phone
- +49 6221 3066
- PRRC contact
- Jens Widmann
EUDAMED certificates
1 certificate1 valid, 0 expiredMDR 1next expiry 18 Jul 2028
BSI Group The Netherlands B.V. 2797 1 certificate
- MDR 742901 Active
Quality management system EU MDR
- Issued
- 4 Aug 2026
- Expires
- 18 Jul 2028
- Reason
- Add device or group
FDA establishments
- Geuder GmbH US
Frequently asked questions
How many devices does Geuder AG have in the registry?
The registry currently lists 7 devices for Geuder AG. Devices recorded under merged duplicate company entries are counted once.
Which registries list Geuder AG's devices?
Among its 7 most recently registered devices, Geuder AG has devices listed in EUDAMED (7 devices).
What risk classes do Geuder AG's devices fall under?
Among its 7 most recently registered devices, the classes recorded for Geuder AG's devices are Class IIa and Class IIb. Each device page shows its own class and authorisation.
What EUDAMED certificates are recorded for Geuder AG?
EUDAMED lists 1 certificate for Geuder AG (quality management system) under MDR. The most recent was issued on 4 Aug 2026.
What are the newest devices from Geuder AG in the registry?
The most recently registered devices listed for Geuder AG include VIVOS device system, Multi-Patient Cassette VIVOS, Footswitch VIVOS and Single-Patient Cassette VIVOS.
Which FDA establishments are linked to Geuder AG?
1 FDA establishment is linked to Geuder AG in the registry; they are listed on the company page.