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Care One

FDA UDI

Class II (US FDA UDI)

by Ahold U.S.A., Inc.

Identity

Trade Name
Care One FDA UDI
Generic Name
Infrared patient thermometer, skin FDA UDI
Device Name
Dual Mode Infrared Thermometer FDA UDI
Model / Reference
FC-IR100 FDA UDI
Description
Dual Mode Infrared Thermometer FDA UDI

Identifiers

Primary DI / UDI-DI
00688267567841 FDA UDI
510(k) Number
K181215 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

No

FDA UDI

Category: Infrared patient thermometer, skin

Care One by Ahold U.S.A., 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
Ahold U.S.A., Inc.

Sources (1)

  • FDA UDI 582575cb-8b00-4d90-bd13-c81486874246 34 fields · synced Jun 8, 2026