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Up & Up

FDA UDI

Class II (US FDA UDI)

by Target Corporation

Identity

Trade Name
Up & Up FDA UDI
Generic Name
Intermittent electronic patient thermometer FDA UDI
Device Name
Up&Up Automatic Digital BP Monitor, Wide-Range Cuff FDA UDI
Model / Reference
094-01-0230 FDA UDI
Description
Up&Up Automatic Digital BP Monitor, Wide-Range Cuff FDA UDI

Identifiers

Catalog Number
48-554 FDA UDI
Primary DI / UDI-DI
00845717009324 FDA UDI
FDA Product Code
FLL FDA UDI
GMDN Term
Intermittent electronic patient thermometer 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: Intermittent electronic patient thermometer

Up & Up by Target Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intermittent electronic patient thermometer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Target Corporation

Sources (1)

  • FDA UDI cc29a252-ac40-4f19-876f-b8bd1ba650a1 34 fields · synced May 30, 2026