Skip to content

Cannulated Screw System + 04.354.024S

by Tyber Medical

Ref 04.354.024S

Cannulated Screw System + 04.354.024S is a device classified as Class IIb in the EU and Class II in the US made by Tyber Medical, registered in EUDAMED on 16 Mar 2026 (Basic UDI-DI 01964490165B) and listed in FDA GUDID since 16 Jun 2021 (UDI-DI 00810080885967), 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 Number01964490165B Basic UDI-DI 00810080885967UDI-DIDate16 Mar 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00810080885967 UDI-DI Date16 Jun 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 01964490165B registered 16 Mar 2026 Active
  • FDA GUDID UDI-DI 00810080885967 listed 16 Jun 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00810080885967
  2. Registered EUDAMED 01964490165B

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  • Withdrawn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
Cannulated Screw System +
Generic name
Orthopaedic bone screw (non-sliding)
Device name
Screws
Model / Ref / Catalog
04.354.024S
Description
2.0MM TI CANN SCREW + LT - 24MM
Primary DI / UDI-DI
00810080885967
Basic UDI-DI
01964490165B
FDA product code
HWC
EMDN code
P09120699 Bone fixation screws, tendon and ligament synthesis screws - other
GMDN term
Orthopaedic bone screw (non-sliding)
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
888.3040
EU registration type
Standard device
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIb
GUDID
Class II

Related devices

Category: Orthopaedic bone screw (non-sliding)

Other devices from Tyber Medical

See all devices from Tyber Medical →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Sutures
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (18, all answered No)