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Frida

FDA UDI

Class II (US FDA UDI)

by Fridababy, LLC

Identity

Trade Name
Frida FDA UDI
Generic Name
Infrared patient thermometer, ear/skin FDA UDI
Device Name
3-in-1 Ear, Forehead, + Touchless Thermometer FDA UDI
Model / Reference
01400100 FDA UDI
Description
3-in-1 Ear, Forehead, + Touchless Thermometer FDA UDI

Identifiers

Catalog Number
100000061 FDA UDI
Primary DI / UDI-DI
00810028778009 FDA UDI
FDA Product Code
SDV FDA UDI
GMDN Term
Infrared patient thermometer, ear/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

Yes

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, ear/skin

Frida by Fridababy, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Infrared patient thermometer, ear/skin.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fridababy, LLC

Sources (1)

  • FDA UDI b6d60d99-602c-4d7f-9d36-82fbc9ae1109 35 fields · synced May 30, 2026