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Shoulder System 04.01.0180

by Medacta International SA

Ref 04.01.0180

Shoulder System 04.01.0180 is a device classified as Class III in the EU and Class II in the US made by Medacta International SA, registered in EUDAMED on 26 Oct 2026 (Basic UDI-DI B-07630040715881), cleared under FDA 510(k) K180089 on 5 Apr 2018 and listed in FDA GUDID since 25 Oct 2021 (UDI-DI 07630040715881), active as of 12 Nov 2026.

Active European Union and United States. Also listed in GUDID (US).

CE MDD 510(k)

Valid until

No date given

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None found

in data synced 12 Nov 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K180089

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-07630040715881 Basic UDI-DI 07630040715881UDI-DIDate26 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07630040715881 UDI-DI Date25 Oct 2021ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK180089 Date5 Apr 2018DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI B-07630040715881 registered 26 Oct 2026 Active
  • FDA 510(k) K180089 decided 5 Apr 2018 Active
  • FDA GUDID UDI-DI 07630040715881 listed 25 Oct 2021 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K180089
  2. Listed FDA GUDID 07630040715881
  3. Registered EUDAMED B-07630040715881

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States FDA 510(k) Active

Specification

EUDAMED · GUDID

Trade name
Short humeral diaphysis - Cementless - 7 EUDAMED
Shoulder System GUDID
Generic name
Total shoulder prosthesis
Device name
Shoulder Humeral diaphysis - Coated
Model / reference
04.01.0180
Primary DI / UDI-DI
07630040715881
Basic UDI-DI
B-07630040715881
510(k) Number
FDA product code
KWS
EMDN code
P0901040202, P0901040204
GMDN term
Total shoulder prosthesis
Device class
Class III EUDAMED
Class II GUDID
Regulation number
888.3660
EU registration type
Legacy device (under a directive)
EU market of registration
Italy
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class III
GUDID
Class II

Device class is stated on each registry's own scale: Class III 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: Total shoulder prosthesis

Cleared under the same submission (K180089)

and 6 more cleared under K180089

Similar devices in this category

Other devices filed under SHOULDER PROSTHESES MODULAR STEMS.

Other devices from Medacta International SA

See all devices from Medacta International SA →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (19, all answered No)