← Back to catalogue

Kroger

FDA UDI

Class II (US FDA UDI)

by Kroger Co., The

Identity

Trade Name
Kroger FDA UDI
Generic Name
Electronic thermometer probe cover FDA UDI
Device Name
KROGER DIGITAL PROBE COVERS ORAL FDA UDI
Model / Reference
112-621-000 FDA UDI
Description
KROGER DIGITAL PROBE COVERS ORAL FDA UDI

Identifiers

Catalog Number
112-621-000 FDA UDI
Primary DI / UDI-DI
00011110350756 FDA UDI
FDA Product Code
FLL FDA UDI
GMDN Term
Electronic thermometer probe cover 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

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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: Electronic thermometer probe cover

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

Similar devices

Also classified as Electronic thermometer probe cover.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Kroger Co., The

Sources (1)

  • FDA UDI 3d177cd1-3b13-4ffb-9e2d-53d43b1b0a89 34 fields · synced May 30, 2026