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Multifunction Unit MR-6000

by Tomey Corporation

Multifunction Unit MR-6000 is a Class I device made by Tomey Corporation, listed in FDA GUDID since 8 Oct 2026 (UDI-DI 04582273613621), 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 Number04582273613621 UDI-DI Date8 Oct 2026ListedStatusListed 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  • Withdrawn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
Multifunction Unit
Generic name
Corneal topography system
Model / reference
MR-6000
Primary DI / UDI-DI
04582273613621
FDA product code
MMQ
GMDN term
Corneal topography system
Device class
Class I
Regulation number
886.1350
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code MMQ (Topographer, Corneal, Ac-Powered).

Other devices from Tomey Corporation

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Properties

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