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Kroger

FDA UDI

Class II (US FDA UDI)

by Kroger Co., The

Identity

Trade Name
Kroger FDA UDI
Generic Name
Continuous electronic patient thermometer, battery-powered FDA UDI
Device Name
KROGER 60 SEC DIG THERM W/BEEPER DUAL SCALE FDA UDI
Model / Reference
112-691-000 FDA UDI
Description
KROGER 60 SEC DIG THERM W/BEEPER DUAL SCALE FDA UDI

Identifiers

Catalog Number
112-691-000 FDA UDI
Primary DI / UDI-DI
00011110793805 FDA UDI
FDA Product Code
FLL FDA UDI
GMDN Term
Continuous electronic patient thermometer, battery-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.2910 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Continuous electronic patient thermometer, battery-powered

Kroger by Kroger Co., The — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Continuous electronic patient thermometer, battery-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kroger Co., The

Sources (1)

  • FDA UDI 08052b8e-e632-49a2-b2ae-bc5346a336e0 34 fields · synced May 31, 2026