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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
Multi-purpose soft/rigid contact lens solution FDA UDI
Device Name
Up & Up 3% hydrogen peroxide Cleaning + disinfecting lens care system (Twin Pack) FDA UDI
Model / Reference
N/A FDA UDI
Description
Up & Up 3% hydrogen peroxide Cleaning + disinfecting lens care system (Twin Pack) FDA UDI

Identifiers

Primary DI / UDI-DI
00095072202025 FDA UDI
FDA Product Code
LPN FDA UDI
GMDN Term
Multi-purpose soft/rigid contact lens solution FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.5928 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multi-purpose soft/rigid contact lens solution

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

Similar devices

Also classified as Multi-purpose soft/rigid contact lens solution.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Target Corporation

Sources (1)

  • FDA UDI b54b45ee-e7d5-4dae-acc3-fc7045bce6e0 33 fields · synced May 30, 2026