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LIGAFIX Chondral pick

by S.B.M

Ref LIG9000190Model Chondral pick

LIGAFIX Chondral pick (LIG9000190) is a Class I device made by S.B.M, registered in EUDAMED on 20 Oct 2023 (Basic UDI-DI 376015400DT201904115K) and listed in FDA GUDID since 20 Jun 2024 (UDI-DI 03760154005685), 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
United StatesGUDID listing GUDID Number03760154005685 UDI-DI Date20 Jun 2024ListedStatusListed GUDID: in commercial distribution
European UnionCE/MDR EUDAMED Number376015400DT201904115K Basic UDI-DI 03760154005685UDI-DIDate20 Oct 2023RegisteredStatusActive

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 376015400DT201904115K registered 20 Oct 2023 Active
  • FDA GUDID UDI-DI 03760154005685 listed 20 Jun 2024 Listed

Timeline

2 dated events

  1. Registered EUDAMED 376015400DT201904115K
  2. Listed FDA GUDID 03760154005685

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  • Withdrawn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
Ligafix® EUDAMED
Ligafix GUDID
Generic name
Endoscopic surgical probe
Model / Ref / Catalog
Chondral pick, LIG9000190
Primary DI / UDI-DI
03760154005685
Basic UDI-DI
376015400DT201904115K
FDA product code
LXH
EMDN code
L091099 Osteosynthesis instruments, reusable - other
GMDN term
Endoscopic surgical probe
Device class
Class I
Regulation number
888.4540
EU registration type
Standard device
EU market of registration
Spain
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Endoscopic surgical probe

Similar devices in this category

Other devices filed under OSTEOSYNTHESIS INSTRUMENTS, REUSABLE - OTHER.

Other devices from S.B.M

See all devices from S.B.M →

Properties

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