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Littmann® CORE®

by Solventum US LLC 4 variants

Ref 8490

Littmann® CORE® (8490) is a Class IIa device made by Solventum US LLC, registered in EUDAMED on 22 Oct 2026 (Basic UDI-DI 01979988401010000000055MU), 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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number01979988401010000000055MU Basic UDI-DI 00197998157011UDI-DIDate22 Oct 2026RegisteredStatusActive

Official records

  • EUDAMED public site Basic UDI-DI 01979988401010000000055MU — open Devices and search for it

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Littmann® CORE® Digital Stethoscope
Model / reference
8490
Primary DI / UDI-DI
00197998157011
Basic UDI-DI
01979988401010000000055MU
EMDN code
C9005 Phonendoscopes and stethoscopes
Device class
Class IIa
System or procedure pack
System which is a device in itself
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)