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MULTIGEN PLUS Knee Tibial Nail Extractor Plier

by Limacorporate

Part of a family of 15 devices: see the family page

Ref 9066.22.180Model MULTIGEN PLUS - Tibial Pin Extractor, 80333901R012ET

MULTIGEN PLUS Knee Tibial Nail Extractor Plier (9066.22.180) is a device classified as Class I in the EU and Class II in the US made by Limacorporate, registered in EUDAMED on 6 Nov 2026 (Basic UDI-DI B-08033390056809), cleared under FDA 510(k) K141934 on 2 Apr 2015 and listed in FDA GUDID since 27 Jul 2016 (UDI-DI 08033390056809), active as of 7 Nov 2026.

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

CE MDR 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 7 Nov 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K141934

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED NumberB-08033390056809 Basic UDI-DI 08033390056809UDI-DIDate6 Nov 2026RegisteredStatusActive
European UnionCE/MDD EUDAMED NumberB-08033390056809 Basic UDI-DI 08033390056809UDI-DIDate6 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number08033390056809 UDI-DI Date27 Jul 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK141934 Date2 Apr 2015DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI B-08033390056809 registered 6 Nov 2026 Active· +1 more in the status table
  • FDA 510(k) K141934 decided 2 Apr 2015 Active
  • FDA GUDID UDI-DI 08033390056809 listed 27 Jul 2016 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K141934
  2. Listed FDA GUDID 08033390056809
  3. Registered EUDAMED B-08033390056809

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
MULTIGEN PLUS - Tibial Pin Extractor EUDAMED
MULTIGEN PLUS Knee GUDID
Generic name
Surgical flat-nosed pliers
Model / Ref / Catalog
MULTIGEN PLUS - Tibial Pin Extractor, 9066.22.180, 80333901R012ET, Tibial Nail Extractor Plier
Primary DI / UDI-DI
08033390056809
Basic UDI-DI
B-08033390056809, 80333901R012ET
510(k) Number
FDA product code
HRY, JWH
EMDN code
L091103 Orthopaedic prostheses forceps, reusable
GMDN term
Surgical flat-nosed pliers
Device class
Class I EUDAMED
Class II GUDID
Regulation number
888.3530, 888.3560
EU registration type
Legacy device (under a directive)
Standard device
EU market of registration
Italy
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
MULTIGEN PLUS - Tibial Pin Extractor
9066.22.180
80333901R012ET
GUDID
Tibial Nail Extractor Plier
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: Surgical flat-nosed pliers

Cleared under the same submission (K141934)

and 8 more cleared under K141934

Similar devices in this category

Other devices filed under ORTHOPAEDIC PROSTHESES FORCEPS, REUSABLE.

Other devices from Limacorporate

See all devices from Limacorporate →

Properties

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