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Discovery 275720000

by Medos International Sàrl

Ref 275720000

Discovery 275720000 is a Class I device made by Medos International Sàrl, registered in EUDAMED on 3 Nov 2026 (Basic UDI-DI B-CHMF000014268000331YH) and listed in FDA GUDID since 31 Dec 2016 (UDI-DI D-CHMF000014268000331YH), 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-CHMF000014268000331YH Basic UDI-DI D-CHMF000014268000331YHUDI-DIDate3 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID NumberD-CHMF000014268000331YH UDI-DI Date31 Dec 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-CHMF000014268000331YH registered 3 Nov 2026 Active
  • FDA GUDID UDI-DI D-CHMF000014268000331YH listed 31 Dec 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID D-CHMF000014268000331YH
  2. Registered EUDAMED B-CHMF000014268000331YH

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  • Withdrawn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
Discovery
Generic name
General internal orthopaedic fixation system implantation kit
Model / Ref / Catalog
275720000
Primary DI / UDI-DI
D-CHMF000014268000331YH EUDAMED
10705034195278 GUDID
Basic UDI-DI
B-CHMF000014268000331YH
FDA product code
LXH
EMDN code
Z12139099 Various orthopaedic and traumatology instruments - other
GMDN term
General internal orthopaedic fixation system implantation kit
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-CHMF000014268000331YH
GUDID
10705034195278

The registries describe this device under different primary UDI-DIs (EUDAMED lists D-CHMF000014268000331YH; FDA GUDID lists 10705034195278), so their flags are not compared.

Related devices

Category: General internal orthopaedic fixation system implantation kit

Similar devices in this category

Other devices filed under VARIOUS ORTHOPAEDIC AND TRAUMATOLOGY INSTRUMENTS - OTHER.

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)