Quick Temp Pro Infrared Thermometer

FDA UDI

Class I (US FDA UDI)

by Home Aide Diagnostics, Inc.

Identity

Trade Name: Quick Temp Pro Infrared Thermometer FDA UDI
Generic Name: Intermittent electronic patient thermometer FDA UDI
Device Name: Quick Temp Pro Infrared Thermometer FDA UDI
Model / Reference: GP-300 FDA UDI
Description: Quick Temp Pro Infrared Thermometer FDA UDI

Identifiers

Primary DI / UDI-DI: 00850632007614 FDA UDI
FDA Product Code: FQZ FDA UDI
GMDN Term: Intermittent electronic patient thermometer FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.2900 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Intermittent electronic patient thermometer

Quick Temp Pro Infrared Thermometer by Home Aide Diagnostics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Home Aide Diagnostics, Inc.

Sources (1)

FDA UDI 64024a57-a22f-474d-b528-e89544167aed 34 fields · synced Jun 8, 2026