Skip to content

Meyco ME610

by Anton Meyer & Co. AG

Meyco ME610 is a Class I device made by Anton Meyer & Co. AG, listed in FDA GUDID since 20 May 2025 (UDI-DI 05060518822568), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05060518822568 UDI-DI Date20 May 2025ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Meyco
Generic name
Ophthalmic knife, reusable
Model / reference
ME610
Primary DI / UDI-DI
05060518822568
FDA product code
HNN
GMDN term
Ophthalmic knife, reusable
Device class
Class I
Regulation number
886.4350
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 knife, reusable.

Other devices from Anton Meyer & Co. AG

See all devices from Anton Meyer & Co. AG →

Properties

  • Sterilise before use
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)