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Walgreens

FDA UDI

Class II (US FDA UDI)

by Walgreen Co.

Identity

Trade Name
Walgreens FDA UDI
Generic Name
Wart-removal cryogenic kit FDA UDI
Device Name
One Step Freeze Wart Remover FDA UDI
Model / Reference
781950 FDA UDI
Description
One Step Freeze Wart Remover FDA UDI

Identifiers

Catalog Number
781950 FDA UDI
Primary DI / UDI-DI
00311917201412 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

Walgreens by Walgreen Co. — 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
Walgreen Co.

Sources (1)

  • FDA UDI 47c4dbce-c5c0-4c8f-8b9c-28c20e628d24 37 fields · synced Jun 8, 2026