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Cougar 292961104

by Depuy Spine, Inc.

Ref 292961104Model Concorde LS Lateral Interbody Instrument System - Reusable Surgical Instruments Elevators, Orthopaedic Surgery

Cougar 292961104 is a Class I device made by Depuy Spine, Inc., registered in EUDAMED on 15 Aug 2025 (Basic UDI-DI 0705034a000715T) and listed in FDA GUDID since 31 Dec 2016 (UDI-DI 10705034226460), active as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0705034a000715T Basic UDI-DI 10705034226460UDI-DIDate15 Aug 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number10705034226460 UDI-DI Date31 Dec 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0705034a000715T registered 15 Aug 2025 Active
  • FDA GUDID UDI-DI 10705034226460 listed 31 Dec 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10705034226460
  2. Registered EUDAMED 0705034a000715T

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  • Withdrawn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
Cougar Ls Lateral Cage System EUDAMED
Cougar GUDID
Generic name
Bone lever/elevator, reusable
Device name
Cobb Elevator
Model / Ref / Catalog
292961104, Concorde LS Lateral Interbody Instrument System - Reusable Surgical Instruments Elevators, Orthopaedic Surgery
Primary DI / UDI-DI
10705034226460
Basic UDI-DI
0705034a000715T
Direct marketing DI
10705034226460
FDA product code
HTE
EMDN code
L0902 Orthopaedic surgery levers, reusable
GMDN term
Bone lever/elevator, reusable
Device class
Class I
Regulation number
878.4800
EU registration type
Standard device
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Bone lever/elevator, reusable

Similar devices in this category

Other devices filed under ORTHOPAEDIC SURGERY LEVERS, REUSABLE.

Other devices from Depuy Spine, Inc.

See all devices from Depuy Spine, Inc. →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (20, all answered No)