Skip to content

Meyco ME425

by Anton Meyer & Co. AG

Ref ME425

Meyco ME425 is a Class I device made by Anton Meyer & Co. AG, registered in EUDAMED on 16 Jun 2026 (Basic UDI-DI B-05060518820205) and listed in FDA GUDID since 20 May 2025 (UDI-DI 05060518820205), active as of 25 Oct 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-05060518820205 Basic UDI-DI 05060518820205UDI-DIDate16 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number05060518820205 UDI-DI Date20 May 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-05060518820205 registered 16 Jun 2026 Active
  • FDA GUDID UDI-DI 05060518820205 listed 20 May 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 05060518820205
  2. Registered EUDAMED B-05060518820205

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  • Withdrawn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
Diamond Knife EUDAMED
Meyco GUDID
Generic name
Ophthalmic knife, reusable
Device name
Diamond Knife (Diamantmesser)
Model / reference
ME425
Primary DI / UDI-DI
05060518820205
Basic UDI-DI
B-05060518820205
FDA product code
HNN
EMDN code
Q02010101 Ophthalmic microknives, straight
GMDN term
Ophthalmic knife, reusable
Device class
Class I
Regulation number
886.4350
System or procedure pack
Procedure pack which is a device in itself
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Ophthalmic knife, reusable

Similar devices in this category

Other devices filed under OPHTHALMIC MICROKNIVES, STRAIGHT.

Other devices from Anton Meyer & Co. AG

See all devices from Anton Meyer & Co. AG →

Properties

  • Sterilise before use
  • Reusable
  • Measuring function
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (17, all answered No)