← Back to catalogue

Mobi

FDA UDI

Class II (US FDA UDI)

by Mobi Technologies, Inc.

Identity

Trade Name
MOBI FDA UDI
Generic Name
Infrared patient thermometer, ear/skin FDA UDI
Device Name
FeverTrack Digital Thermometer FDA UDI
Model / Reference
70116 FDA UDI
Description
FeverTrack Digital Thermometer FDA UDI

Identifiers

Primary DI / UDI-DI
00891040701169 FDA UDI
FDA Product Code
FLL 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

Yes

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, ear/skin

Mobi by Mobi Technologies, Inc. — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI e01dd134-0b0e-4f4b-96a7-92a186feda0e 35 fields · synced Jun 1, 2026