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Kroger 112-691-000

by Kroger Co., the

Kroger 112-691-000 is a Class II device made by Kroger Co., the, listed in FDA GUDID since 18 Jul 2016 (UDI-DI 00011110793805), 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 Number00011110793805 UDI-DI Date18 Jul 2016ListedStatusListed 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  • Withdrawn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
Kroger
Generic name
Continuous electronic patient thermometer, battery-powered
Model / Ref / Catalog
112-691-000
Primary DI / UDI-DI
00011110793805
FDA product code
FLL
GMDN term
Continuous electronic patient thermometer, battery-powered
Device class
Class II
Regulation number
880.2910
GUDID distribution status
In Commercial Distribution

Related devices

Category: Continuous electronic patient thermometer, battery-powered

Similar devices

Other devices filed under FDA product code FLL (Thermometer, Electronic, Clinical).

Other devices from Kroger Co., the

See all devices from Kroger Co., the →

Properties

  • Lot / batch number
Other properties (14, all answered No)