← Back to catalogue

W.W. Grainger, Inc.,

FDA UDI

Class II (US FDA UDI)

by Grainger International, Inc.

Identity

Trade Name
W.W. Grainger, Inc., FDA UDI
Generic Name
Infrared patient thermometer, skin FDA UDI
Device Name
Non-Contact Forehead Thermometer FDA UDI
Model / Reference
THD2FE FDA UDI
Description
Non-Contact Forehead Thermometer FDA UDI

Identifiers

Catalog Number
56JN58 FDA UDI
Primary DI / UDI-DI
00194484319427 FDA UDI
FDA Product Code
FLL FDA UDI
GMDN Term
Infrared patient thermometer, skin 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

Yes

FDA UDI

Category: Infrared patient thermometer, skin

W.W. Grainger, Inc., by Grainger International, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Infrared patient thermometer, skin.

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

Sources (1)

  • FDA UDI 451417ae-9a99-4919-90bd-39a91aff68f7 34 fields · synced May 30, 2026