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Spine Instruments 03.65.10.0037

by Medacta International

Ref 03.65.10.0037

Spine Instruments 03.65.10.0037 is a device classified as Class IIa in the EU and Class I in the US made by Medacta International, registered in EUDAMED on 27 Oct 2026 (Basic UDI-DI B-07630971213388) and listed in FDA GUDID since 2 Dec 2020 (UDI-DI 07630971213388), active as of 7 Nov 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-07630971213388 Basic UDI-DI 07630971213388UDI-DIDate27 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07630971213388 UDI-DI Date2 Dec 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-07630971213388 registered 27 Oct 2026 Active
  • FDA GUDID UDI-DI 07630971213388 listed 2 Dec 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07630971213388
  2. Registered EUDAMED B-07630971213388

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  • Withdrawn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
Web.a Screwdriver EUDAMED
Spine Instruments GUDID
Generic name
Orthopaedic surgical procedure kit, non-medicated, reusable
Device name
Spine Screwdriver
Model / reference
03.65.10.0037
Primary DI / UDI-DI
07630971213388
Basic UDI-DI
B-07630971213388
FDA product code
LXH
EMDN code
Z12130599 Motorised orthopaedic surgery system instruments - other
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

Related devices

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

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)