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ATI, Inc.

FDA UDI

Class II (US FDA UDI)

by American Thermal Instruments, Llc

Identity

Trade Name
ATI, Inc. FDA UDI
Generic Name
Colour-indication patient thermometer FDA UDI
Device Name
Disposable Forehead Thermometer FDA UDI
Model / Reference
C-8786 FDA UDI
Description
Disposable Forehead Thermometer FDA UDI

Identifiers

Primary DI / UDI-DI
00029431000045 FDA UDI
FDA Product Code
KPD FDA UDI
GMDN Term
Colour-indication patient thermometer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.2200 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Colour-indication patient thermometer

ATI, Inc. by American Thermal Instruments, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Colour-indication patient thermometer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 43116ae9-0098-4a06-88a8-45c073e15536 33 fields · synced Jun 8, 2026