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Führung

by Peter Brehm GmbH 5 variants

Part of a family of 85 devices: see the family page

Ref 54844-30

Führung (54844-30) is a Class I device made by Peter Brehm GmbH, registered in EUDAMED on 11 Aug 2026 (Basic UDI-DI 4029839PB00000087H), active as of 24 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4029839PB00000087H Basic UDI-DI 04029839145351UDI-DIDate11 Aug 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
MRS-TITAN Comfort Instruments
Model / reference
54844-30
Primary DI / UDI-DI
04029839145351
Basic UDI-DI
4029839PB00000087H
EMDN code
L091199 Orthopaedic prosthetics instruments, reusable - other
Device class
Class I
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000006458

Similar devices in this category

Other devices filed under ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER.

Other devices from Peter Brehm GmbH

See all devices from Peter Brehm GmbH →

Properties

  • Sterilise before use
  • Reusable
  • Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction)
Other properties (11, all answered No)