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MOVE 78 Cold & Flu Kit

FDA UDI

Class II (US FDA UDI)

by Trend Power Limited

Identity

Trade Name
MOVE 78 Cold & Flu Kit FDA UDI
Generic Name
Pulse oximeter FDA UDI
Device Name
MOVE 78 Cold & Flu Kit comprises of a Touchless Infrared thermometer and a pulse oximeter. Both devices are bluetooth enabled. FDA UDI
Model / Reference
MOVE78-ESS FDA UDI
Description
MOVE 78 Cold & Flu Kit comprises of a Touchless Infrared thermometer and a pulse oximeter. Both devices are bluetooth enabled. FDA UDI

Identifiers

Primary DI / UDI-DI
00850031915053 FDA UDI
FDA Product Code
FLL FDA UDI
OCH FDA UDI
GMDN Term
Pulse oximeter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.2910 FDA UDI
870.2700 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, skinPulse oximeter

MOVE 78 Cold & Flu Kit by Trend Power Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pulse oximeter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Trend Power Limited

Sources (1)

  • FDA UDI c47ba21a-e4aa-480e-b7e7-d9629002fd26 33 fields · synced May 30, 2026