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Expedium Verse 299704205

by Medos International Sàrl

Ref 299704205

Expedium Verse 299704205 is a Class I device made by Medos International Sàrl, registered in EUDAMED on 3 Nov 2026 (Basic UDI-DI B-CHMF000014268000319YT) and listed in FDA GUDID since 31 Dec 2016 (UDI-DI D-CHMF000014268000319YT), active as of 7 Nov 2026.

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

CE MDD

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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-CHMF000014268000319YT Basic UDI-DI D-CHMF000014268000319YTUDI-DIDate3 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID NumberD-CHMF000014268000319YT UDI-DI Date31 Dec 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-CHMF000014268000319YT registered 3 Nov 2026 Active
  • FDA GUDID UDI-DI D-CHMF000014268000319YT listed 31 Dec 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID D-CHMF000014268000319YT
  2. Registered EUDAMED B-CHMF000014268000319YT

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Expedium Verse
Generic name
Orthopaedic inorganic implant inserter/extractor, reusable
Model / Ref / Catalog
299704205
Primary DI / UDI-DI
D-CHMF000014268000319YT EUDAMED
10705034467511 GUDID
Basic UDI-DI
B-CHMF000014268000319YT
FDA product code
LXH
EMDN code
L091001 Instruments for insertion and extraction of materials for osteosynthesis, reusable
GMDN term
Orthopaedic inorganic implant inserter/extractor, reusable
Device class
Class I
Regulation number
888.4540
EU registration type
Legacy device (under a directive)
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
D-CHMF000014268000319YT
GUDID
10705034467511

The registries describe this device under different primary UDI-DIs (EUDAMED lists D-CHMF000014268000319YT; FDA GUDID lists 10705034467511), so their flags are not compared.

Related devices

Category: Orthopaedic inorganic implant inserter/extractor, reusable

Similar devices in this category

Other devices filed under INSTRUMENTS FOR INSERTION AND EXTRACTION OF MATERIALS FOR OSTEOSYNTHESIS, REUSABLE.

Other devices from Medos International SARL

See all devices from Medos International SARL →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (20, all answered No)