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Well at Walgreens

FDA UDI

Class II (US FDA UDI)

by Walgreen Co.

Identity

Trade Name
Well at Walgreens FDA UDI
Generic Name
Intermittent electronic patient thermometer FDA UDI
Device Name
Walgreens Quick Read Digital Thermometer FDA UDI
Model / Reference
KD-113 FDA UDI
Description
Walgreens Quick Read Digital Thermometer FDA UDI

Identifiers

Catalog Number
268691 FDA UDI
Primary DI / UDI-DI
00311917157603 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

Well at Walgreens by Walgreen Co. — 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
Walgreen Co.

Sources (1)

  • FDA UDI 7d8bf273-b2f2-4e58-8cb6-bd58e0ec6200 35 fields · synced May 31, 2026