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6173.0110

by Globus Medical, Inc.

Ref 6173.0110

6173.0110 is a Class I device made by Globus Medical, Inc., registered in EUDAMED on 8 May 2026 (Basic UDI-DI 0193982NONINVINSTLT) and listed in FDA GUDID since 10 Jul 2019 (UDI-DI 00889095660906), active as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0193982NONINVINSTLT Basic UDI-DI 00889095660906UDI-DIDate8 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00889095660906 UDI-DI Date10 Jul 2019ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0193982NONINVINSTLT registered 8 May 2026 Active
  • FDA GUDID UDI-DI 00889095660906 listed 10 Jul 2019 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00889095660906
  2. Registered EUDAMED 0193982NONINVINSTLT

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  • Withdrawn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

Generic name
Surgical torque wrench, reusable
Device name
Non-Invasive Instruments
Model / reference
6173.0110
Primary DI / UDI-DI
00889095660906
Basic UDI-DI
0193982NONINVINSTLT
Direct marketing DI
00889095660906
FDA product code
LXH
EMDN code
L0902 Orthopaedic surgery levers, reusable
GMDN term
Surgical torque wrench, reusable
Device class
Class I
Regulation number
888.4540
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Surgical torque wrench, reusable

Similar devices in this category

Other devices filed under ORTHOPAEDIC SURGERY LEVERS, REUSABLE.

Other devices from Globus Medical, Inc.

See all devices from Globus Medical, Inc. →

Properties

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