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Clarifi Imaging System

by Modulated Imaging Inc.

Clarifi Imaging System is a Class II device made by Modulated Imaging Inc., listed in FDA GUDID since 21 Dec 2018 (UDI-DI 00859806007023), registry data as of 8 Nov 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 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00859806007023 UDI-DI Date21 Dec 2018ListedStatusListed 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  • Withdrawn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

Generic name
Tissue saturation oximeter
Model / reference
Clarifi
Primary DI / UDI-DI
00859806007023
FDA product code
MUD
GMDN term
Tissue saturation oximeter
Device class
Class II
Regulation number
870.2700
GUDID distribution status
In Commercial Distribution

Related devices

Category: Tissue saturation oximeter

Other devices from Modulated Imaging Inc.

Properties

  • Prescription use
  • Serial number
Other properties (13, all answered No)