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Schlumbohm GmbH & Co. KG

Active in EUDAMED

Germanyfrom SRN EUDAMED FDA SRN DE-MF-000005266 FEI 3018783058

Devices
4
Registrations
EUDAMEDFDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

EU certificates

1 of 1 in force.

See certificates

Market reach

European Union
EUDAMED actor, 1 certificate
United States
FDA FEI

What Schlumbohm GmbH & Co. KG makes

Schlumbohm GmbH & Co. KG manufactures a range of endomotor and bone processing devices, including the EndoPilot comfort endomotor, the KF‑T3 system, the Knochenmühle bone mill, the KnochenFilter KF‑T3 bone filter, and the Knochenmühle KM‑3 bone mill variant.

All of these devices are classified as Class IIa medical devices and are listed in the European Union database (Eudamed). The company is based in Germany.

AI-generated from registry data, 5 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue4

Newest first, rows 1-4 of 4

  • Knochenmühle Ref 108 0030

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • KnochenFilter KF-T3 Ref 104 3100

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa
  • Knochenmühle KM-3 Ref 108 0030

    Active Regimes: CE MDD Registry: EUDAMED Class:IIa
  • EndoPilot comfort Ref 110 0101

    Active Regimes: CE MDR 510(k) Registry: EUDAMED Class:IIa

Company details

EUDAMED SRN
DE-MF-000005266
FDA FEI number
3018783058
EU VAT number
DE811513248
EUDAMED status
Active
EUDAMED registered name
Schlumbohm GmbH & Co. KG
EUDAMED abbreviated name
Schlumbohm
Registered address
8-10, Klein Floyen, 24616, Brokstedt, Germany
Phone
+49-43248929-0
PRRC contact
Gerald Schlumbohm(public in EUDAMED)

EUDAMED certificates1

1 certificate1 valid, 0 expiredMDR 1next expiry 8 Apr 2030

EUDAMED certificates (1)

DNV MEDCERT GmbH 0482 1 certificate

  • 1712GB448250912 Active

    Quality management system EU MDR

    Issued
    12 Sep 2025
    Expires
    8 Apr 2030

Frequently asked questions

How many devices does Schlumbohm GmbH & Co. KG have in the registry?

The registry currently lists 4 devices for Schlumbohm GmbH & Co. KG. Devices recorded under merged duplicate company entries are counted once.

Which registries list Schlumbohm GmbH & Co. KG's devices?

Among its 4 most recently registered devices, Schlumbohm GmbH & Co. KG has devices listed in EUDAMED (4 devices).

What risk classes do Schlumbohm GmbH & Co. KG's devices fall under?

Among its 4 most recently registered devices, the classes recorded for Schlumbohm GmbH & Co. KG's devices are Class IIa. Each device page shows its own class and authorisation.

What EUDAMED certificates are recorded for Schlumbohm GmbH & Co. KG?

EUDAMED lists 1 certificate for Schlumbohm GmbH & Co. KG (quality management system) under MDR. 1 is recorded with the status issued. The most recent was issued on 12 Sep 2025.

What are the newest devices from Schlumbohm GmbH & Co. KG in the registry?

The most recently registered devices listed for Schlumbohm GmbH & Co. KG include Knochenmühle, KnochenFilter KF-T3, Knochenmühle KM-3 and EndoPilot comfort.

Generated automatically from registry data and not verified by a human reviewer.