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ThermoWorks WAND Blue

FDA UDI

Class II (US FDA UDI)

by Thermoworks Inc.

Identity

Trade Name
ThermoWorks WAND Blue FDA UDI
Generic Name
Infrared patient thermometer, skin FDA UDI
Device Name
Bluetooth Forehead Thermometer, infrared FDA UDI
Model / Reference
THD2FE-B FDA UDI
Description
Bluetooth Forehead Thermometer, infrared FDA UDI

Identifiers

Primary DI / UDI-DI
00860003705315 FDA UDI
510(k) Number
K121428 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Infrared patient thermometer, skin

ThermoWorks WAND Blue by Thermoworks Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Infrared patient thermometer, skin.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Thermoworks Inc.

Sources (1)

  • FDA UDI ea837874-7ca5-42c6-a54d-cae06e8d62b8 34 fields · synced Jun 6, 2026