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Aesculap MB666R

by Aesculap, Inc.

Part of a family of 341 devices: see the family page

Ref MB666R

Aesculap MB666R is a Class I device made by Aesculap, Inc., registered in EUDAMED on 16 Sep 2025 (Basic UDI-DI 403923900000044325) and listed in FDA GUDID since 6 May 2020 (UDI-DI 04046963364878), active as of 22 Oct 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number403923900000044325 Basic UDI-DI 04046963364878UDI-DIDate16 Sep 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number04046963364878 UDI-DI Date6 May 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 403923900000044325 registered 16 Sep 2025 Active
  • FDA GUDID UDI-DI 04046963364878 listed 6 May 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04046963364878
  2. Registered EUDAMED 403923900000044325

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  • Withdrawn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
Aesculap
Generic name
Orthopaedic osteotome
Device name
Chisel / osteotome
Model / Ref / Catalog
MB666R
Primary DI / UDI-DI
04046963364878
Basic UDI-DI
403923900000044325
Direct marketing DI
04046963364878
FDA product code
GFI
EMDN code
L090401 Orthopaedic surgery osteotomes, reusable
GMDN term
Orthopaedic osteotome
Device class
Class I
Regulation number
878.4800
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices in this category

Other devices filed under ORTHOPAEDIC SURGERY OSTEOTOMES, REUSABLE.

Other devices from Aesculap, Inc.

See all devices from Aesculap, Inc. →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (20, all answered No)