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Idys™- ALIF 24741000

by Clariance, Inc.

Ref 24741000Model Spinal instrumentation

Idys™- ALIF 24741000 is a Class I device made by Clariance, Inc., registered in EUDAMED on 7 Jul 2026 (Basic UDI-DI 0370078069981DILF4) and listed in FDA GUDID since 6 Jun 2018 (UDI-DI 03700780610525), active as of 25 Oct 2026.

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

CE MDR

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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0370078069981DILF4 Basic UDI-DI 03700780610525UDI-DIDate7 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number03700780610525 UDI-DI Date6 Jun 2018ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0370078069981DILF4 registered 7 Jul 2026 Active
  • FDA GUDID UDI-DI 03700780610525 listed 6 Jun 2018 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 03700780610525
  2. Registered EUDAMED 0370078069981DILF4

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
Distracteur Intervertebral EUDAMED
Idys™- ALIF GUDID
Generic name
Orthopaedic surgical procedure kit, non-medicated, reusable
Model / Ref / Catalog
24741000, Spinal instrumentation
Primary DI / UDI-DI
03700780610525
Basic UDI-DI
0370078069981DILF4
FDA product code
HTD
EMDN code
P090799 Spinal prostheses and stabilisation systems - other
GMDN term
Orthopaedic surgical procedure kit, non-medicated, reusable
Device class
Class I
Regulation number
878.4800
EU registration type
Standard device
EU market of registration
France
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

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

Similar devices in this category

Other devices filed under SPINAL PROSTHESES AND STABILISATION SYSTEMS - OTHER.

Other devices from Clariance, Inc.

See all devices from Clariance, Inc. →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (19, all answered No)