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Mdf® MDF767BO

by MDF Instruments Medifriend Inc.

Part of a family of 8 devices: see the family page

Ref MDF767BOModel MDF 767

Mdf® MDF767BO is a Class I device made by MDF Instruments Medifriend Inc., registered in EUDAMED on 22 Oct 2026 (Basic UDI-DI 69402116767RA) and listed in FDA GUDID since 1 Aug 2019 (UDI-DI 06940211619155), 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 Number69402116767RA Basic UDI-DI 06940211619155UDI-DIDate22 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number06940211619155 UDI-DI Date1 Aug 2019ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 69402116767RA registered 22 Oct 2026 Active
  • FDA GUDID UDI-DI 06940211619155 listed 1 Aug 2019 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 06940211619155
  2. Registered EUDAMED 69402116767RA

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  • Withdrawn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
Mdf®
Generic name
Mechanical external stethoscope
Device name
MDF® Sprague Rappaport Stethoscope
Model / reference
MDF767BO, MDF 767
Primary DI / UDI-DI
06940211619155
Basic UDI-DI
69402116767RA
FDA product code
LDE
EMDN code
C9005 Phonendoscopes and stethoscopes
GMDN term
Mechanical external stethoscope
Device class
Class I
Regulation number
870.1875
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Related devices

Category: Mechanical external stethoscope

Similar devices in this category

Other devices filed under PHONENDOSCOPES AND STETHOSCOPES.

Other devices from MDF Instruments Medifriend Inc.

See all devices from MDF Instruments Medifriend Inc. →

Properties

  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (22, all answered No)