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Diamond Knife

by Anton Meyer & Co. AG

Ref ME100, A-513, ME420MAModel REIHE: A-200, A-300, A-500, A-800, A-N200, A-NANO

Diamond Knife (ME100) is a Class I device made by Anton Meyer & Co. AG, registered in EUDAMED on 6 May 2026 (Basic UDI-DI B-05060518820014) and listed in FDA GUDID since 24 Sep 2023 (UDI-DI 05060518820014), active as of 22 Oct 2026.

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

CE MDR 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED NumberB-05060518820014 Basic UDI-DI Date6 May 2026RegisteredStatusActive
European UnionCE/MDD EUDAMED NumberB-05060518820014 Basic UDI-DI Date6 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number05060518820014 UDI-DI Date24 Sep 2023ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-05060518820014 registered 6 May 2026 Active· +1 more in the status table
  • FDA GUDID UDI-DI 05060518820014 listed 24 Sep 2023 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 05060518820014
  2. Registered EUDAMED B-05060518820014

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR, 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
ME100, ME420MA, REIHE: A-200, A-300, A-500, A-800, A-N200, A-NANO, A-513
Primary DI / UDI-DI
05060518820014, 05060518822414, 05060570982460
Basic UDI-DI
B-05060518820014, 506057098A-NE, B-05060518822414
Direct marketing DI
05060570982460
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)
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Manufacturer details

EUDAMED SRN
CH-MF-000040740
Authorised representative
MDSS GmbH DE-AR-000005430

Similar devices in this category

Other devices filed under OPHTHALMIC MICROKNIVES, STRAIGHT.

Other devices from Anton Meyer & Co. AG

Properties

  • Sterilise before use
  • Reusable
  • Measuring function NoEUDAMEDYesEUDAMED
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (19, all answered No)