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MobiliT Cup MDM052A

by Corin Ltd

Ref MDM052AModel MobiliT™ Cup Instrument System

MobiliT Cup MDM052A is a device classified as Class I in the EU and Class II in the US made by Corin Ltd, registered in EUDAMED on 14 Oct 2026 (Basic UDI-DI B-05056139240935), cleared under FDA 510(k) K191831 on 16 Jan 2020 and listed in FDA GUDID since 8 Dec 2022 (UDI-DI 05056139240935), active as of 24 Oct 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 24 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K191831

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-05056139240935 Basic UDI-DI 05056139240935UDI-DIDate14 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number05056139240935 UDI-DI Date8 Dec 2022ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK191831 Date16 Jan 2020DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI B-05056139240935 registered 14 Oct 2026 Active
  • FDA 510(k) K191831 decided 16 Jan 2020 Active
  • FDA GUDID UDI-DI 05056139240935 listed 8 Dec 2022 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K191831
  2. Listed FDA GUDID 05056139240935
  3. Registered EUDAMED B-05056139240935

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  • Withdrawn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
Cup holder attachment PEEK Ø52 EUDAMED
MobiliT Cup GUDID
Generic name
Orthopaedic implant impactor, reusable
Model / Ref / Catalog
MDM052A, MobiliT™ Cup Instrument System
Primary DI / UDI-DI
05056139240935
Basic UDI-DI
B-05056139240935
510(k) Number
FDA product code
MEH, LZO
EMDN code
L0999 Orthopaedic and traumatological surgery instruments, reusable - other
GMDN term
Orthopaedic implant impactor, reusable
Device class
Class I EUDAMED
Class II GUDID
Regulation number
888.3353
EU registration type
Legacy device (under a directive)
EU market of registration
France
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I 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: Orthopaedic implant impactor, reusable

Cleared under the same submission (K191831)

and 8 more cleared under K191831

Similar devices in this category

Other devices filed under ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER.

Other devices from Corin Ltd

See all devices from Corin Ltd →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Lot / batch number
Other properties (21, all answered No)