Skip to content

6173.1504

by Globus Medical, Inc.

Ref 6173.1504

6173.1504 is a Class I device made by Globus Medical, Inc., registered in EUDAMED on 23 Jun 2026 (Basic UDI-DI 0193982INSTRUMENTSKC) with CE/MDR certificate 1000315034 valid until 14 May 2029 and listed in FDA GUDID since 10 Jul 2019 (UDI-DI 00889095717655), active as of 24 Oct 2026.

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

CE MDR

Valid until

14 May 2029

CE MDR certificate

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

1 certificate

Certifier DQS Medizinprodukte GmbH

Trust

Unverified

Source EUDAMED, GUDID, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0193982INSTRUMENTSKC Basic UDI-DI 00889095717655UDI-DIDate23 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00889095717655 UDI-DI Date10 Jul 2019ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0193982INSTRUMENTSKC registered 23 Jun 2026 Active· +1 more in the status table
  • FDA GUDID UDI-DI 00889095717655 listed 10 Jul 2019 Listed

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 1000315034 Active Supplemented

    Quality management system EU MDR

    Certifier
    DQS Medizinprodukte GmbH 0297
    Issued
    10 Jun 2026
    Expires
    14 May 2029
    Reason
    Add device or group

Timeline

4 dated events

  1. Listed FDA GUDID 00889095717655
  2. Certificate issued EUDAMED 1000315034
  3. Registered EUDAMED 0193982INSTRUMENTSKC
  4. Certificate expires EUDAMED 1000315034

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  • Withdrawn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
ARBOR External Fixation
Generic name
Fluted surgical drill bit, reusable
Device name
Reusable Instruments
Model / reference
6173.1504
Primary DI / UDI-DI
00889095717655
Basic UDI-DI
0193982INSTRUMENTSKC
Direct marketing DI
00889095717655
FDA product code
LXH
EMDN code
L0999 Orthopaedic and traumatological surgery instruments, reusable - other
GMDN term
Fluted surgical drill bit, 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

Similar devices in this category

Other devices filed under ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER.

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)