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Verticale

by Silony Medical GmbH 137 variants

Part of a family of 9 devices: see the family page

Ref VI-5450

Verticale (VI-5450) is a Class I device made by Silony Medical GmbH, registered in EUDAMED on 20 May 2026 (Basic UDI-DI 4054896FRAMESWQ) and listed in FDA GUDID since 18 Sep 2026 (UDI-DI 04054896079530), 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 Number04054896079530 UDI-DI Date18 Sep 2026ListedStatusListed GUDID: in commercial distribution
European UnionCE/MDR EUDAMED Number4054896FRAMESWQ Basic UDI-DI 04054896079530UDI-DIDate20 May 2026RegisteredStatusActive

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 4054896FRAMESWQ registered 20 May 2026 Active
  • FDA GUDID UDI-DI 04054896079530 listed 18 Sep 2026 Listed

Timeline

2 dated events

  1. Registered EUDAMED 4054896FRAMESWQ
  2. Listed FDA GUDID 04054896079530

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  • Withdrawn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
Verticale EUDAMED
Frames GUDID
Generic name
General internal orthopaedic fixation system implantation kit
Device name
Frame
Model / Ref / Catalog
VI-5450
Primary DI / UDI-DI
04054896079530
Basic UDI-DI
4054896FRAMESWQ
FDA product code
LXH
EMDN code
L091199 Orthopaedic prosthetics instruments, reusable - other
GMDN term
General internal orthopaedic fixation system implantation kit
Device class
Class I
Regulation number
888.4540
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Manufacturer details

EUDAMED SRN
DE-MF-000006463

Similar devices in this category

Other devices filed under ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER.

Other devices from Silony Medical GmbH

See all devices from Silony Medical GmbH →

Properties

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