← Back to catalogue

Relion

FDA UDI

Class II (US FDA UDI)

by Walmart Stores

Identity

Trade Name
RELION FDA UDI
Generic Name
Continuous electronic patient thermometer, battery-powered FDA UDI
Device Name
RELION BASAL DIGITAL THERM FDA UDI
Model / Reference
144-639-000 FDA UDI
Description
RELION BASAL DIGITAL THERM FDA UDI

Identifiers

Catalog Number
144-639-000 FDA UDI
Primary DI / UDI-DI
00681131060271 FDA UDI
510(k) Number
K962520 FDA UDI
FDA Product Code
OZK 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

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: Continuous electronic patient thermometer, battery-powered

Relion by Walmart Stores — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Cleared under the same submission

K962520 also covers:

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
Walmart Stores

Sources (1)

  • FDA UDI 699e0a0a-533c-4ff4-8b33-e96a94afc8f1 35 fields · synced Jun 1, 2026