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3M™ Littmann® 8869

by 3M Company

Ref 8869

3M™ Littmann® 8869 is a device classified as Class IIa in the EU and Class II in the US made by 3M Company, registered in EUDAMED on 22 Oct 2026 (Basic UDI-DI 06082238401010000000055AK) and listed in FDA GUDID since 1 Jun 2023 (UDI-DI 00707387812645), active as of 7 Nov 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number06082238401010000000055AK Basic UDI-DI 00707387812645UDI-DIDate22 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00707387812645 UDI-DI Date1 Jun 2023ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 06082238401010000000055AK registered 22 Oct 2026 Active
  • FDA GUDID UDI-DI 00707387812645 listed 1 Jun 2023 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00707387812645
  2. Registered EUDAMED 06082238401010000000055AK

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
3M™ Littmann®
Generic name
Electronic acoustic stethoscope
Model / Ref / Catalog
8869
Primary DI / UDI-DI
00707387812645
Basic UDI-DI
06082238401010000000055AK
FDA product code
DQD
EMDN code
C9005 Phonendoscopes and stethoscopes
GMDN term
Electronic acoustic stethoscope
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
870.1875
System or procedure pack
System which is a device in itself
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class II

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Electronic acoustic stethoscope

Similar devices in this category

Other devices filed under PHONENDOSCOPES AND STETHOSCOPES.

Other devices from 3M Company

See all devices from 3M Company →

Properties

  • Over-the-counter
  • Lot / batch number
  • Manufacturing date
Other properties (22, all answered No)