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Equaline

FDA UDI

Class II (US FDA UDI)

by Supervalu Inc.

Identity

Trade Name
EQUALINE FDA UDI
Generic Name
Intermittent electronic patient thermometer FDA UDI
Device Name
A hand-held, battery-powered, electronic instrument designed for oral, under arm or rectal use to to measure a patient's body temperature. The device has a rigid tip and an LCD display. It is designed to take a temperature reading in approximately 30 seconds. This is a reusable device. FDA UDI
Model / Reference
KD-1351 FDA UDI
Description
A hand-held, battery-powered, electronic instrument designed for oral, under arm or rectal use to to measure a patient's body temperature. The device has a rigid tip and an LCD display. It is designed to take a temperature reading in approximately 30 seconds. This is a reusable device. FDA UDI

Identifiers

Primary DI / UDI-DI
00041163495784 FDA UDI
FDA Product Code
FLL FDA UDI
GMDN Term
Intermittent electronic patient thermometer 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

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: Intermittent electronic patient thermometer

Equaline by Supervalu Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intermittent electronic patient thermometer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Supervalu Inc.

Sources (1)

  • FDA UDI b6d43f23-67e7-4618-9ebe-c84298448213 34 fields · synced May 30, 2026