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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
Wart-removal cryogenic kit FDA UDI
Device Name
Wart Freezer One Step Wart Remover FDA UDI
Model / Reference
245060245 FDA UDI
Description
Wart Freezer One Step Wart Remover FDA UDI

Identifiers

Catalog Number
245060245 FDA UDI
Primary DI / UDI-DI
00017276228489 FDA UDI
FDA Product Code
GEH FDA UDI
GMDN Term
Wart-removal cryogenic kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4350 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Height — 155 Millimeter FDA UDI

Category: Wart-removal cryogenic kit

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

Similar devices

Also classified as Wart-removal cryogenic kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Target Corporation

Sources (1)

  • FDA UDI 0efa9221-8fa8-4760-8495-a1bbc8d6ac0c 37 fields · synced May 30, 2026