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UltrOx 610-2472

by Civco Medical Instruments Co., Inc.

UltrOx 610-2472 is a Class II device made by Civco Medical Instruments Co., Inc., listed in FDA GUDID since 3 May 2023 (UDI-DI 10841436123140), 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 Number10841436123140 UDI-DI Date3 May 2023ListedStatusListed 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  • Withdrawn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
UltrOx
Generic name
Hydrogen peroxide device disinfectant/sterilant test strip
Model / Ref / Catalog
610-2472
Primary DI / UDI-DI
10841436123140
FDA product code
JOJ
GMDN term
Hydrogen peroxide device disinfectant/sterilant test strip
Device class
Class II
Regulation number
880.2800
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code JOJ (Indicator, physical/chemical sterilization process).

Other devices from Civco Medical Instruments Co., Inc.

See all devices from Civco Medical Instruments Co., Inc. →

Properties

  • Single use
  • Over-the-counter
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)