Skip to content

Littmann®

by Solventum US LLC 14 variants

Ref 2454

Littmann® (2454) is a Class I device made by Solventum US LLC, registered in EUDAMED on 22 Oct 2026 (Basic UDI-DI 01979988401010000000033MJ), active as of 7 Nov 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, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number01979988401010000000033MJ Basic UDI-DI 00197998184710UDI-DIDate22 Oct 2026RegisteredStatusActive

Official records

  • EUDAMED public site Basic UDI-DI 01979988401010000000033MJ — open Devices and search for it

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Littmann® Lightweight II S.E. Stethoscope
Model / reference
2454
Primary DI / UDI-DI
00197998184710
Basic UDI-DI
01979988401010000000033MJ
EMDN code
C9005 Phonendoscopes and stethoscopes
Device class
Class I
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
US-MF-000044314
Authorised representative
Solventum Germany GmbH DE-AR-000043541

Similar devices in this category

Other devices filed under PHONENDOSCOPES AND STETHOSCOPES.

Other devices from Solventum US LLC

See all devices from Solventum US LLC →

Properties

Other properties (14, all answered No)