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Hip Instruments 01.10.10.0620

by Medacta International

Ref 01.10.10.0620Model Hip Trial head

Hip Instruments 01.10.10.0620 is a device classified as Class IIa in the EU and Class I in the US made by Medacta International, registered in EUDAMED on 23 Jul 2026 (Basic UDI-DI B-07630040741323) and listed in FDA GUDID since 20 Apr 2021 (UDI-DI 07630040741323), active as of 23 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDD

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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-07630040741323 Basic UDI-DI 07630040741323UDI-DIDate23 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07630040741323 UDI-DI Date20 Apr 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-07630040741323 registered 23 Jul 2026 Active
  • FDA GUDID UDI-DI 07630040741323 listed 20 Apr 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07630040741323
  2. Registered EUDAMED B-07630040741323

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Trial Head diam. 32 #XL EUDAMED
Hip Instruments GUDID
Generic name
Orthopaedic surgical procedure kit, non-medicated, reusable
Model / reference
01.10.10.0620, Hip Trial head
Primary DI / UDI-DI
07630040741323
Basic UDI-DI
B-07630040741323
FDA product code
LXH
EMDN code
V06010101 Hip prostheses testing devices
GMDN term
Orthopaedic surgical procedure kit, non-medicated, reusable
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
888.4540
EU registration type
Legacy device (under a directive)
EU market of registration
Italy
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 IIa
GUDID
Class I

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class I in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Orthopaedic surgical procedure kit, non-medicated, reusable

Similar devices in this category

Other devices filed under ORTHOPAEDIC PROSTHESES TESTING DEVICES.

Other devices from Medacta International

See all devices from Medacta International →

Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
Other properties (22, all answered No)