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CVS Health

FDA UDI

Class II (US FDA UDI)

by Woonsocket Prescription Center, Incorporated

Identity

Trade Name
CVS Health FDA UDI
Generic Name
Wart-removal cryogenic kit FDA UDI
Device Name
Ready to Use Wart Freezer Cryogenic Treatment FDA UDI
Model / Reference
717272 FDA UDI
Description
Ready to Use Wart Freezer Cryogenic Treatment FDA UDI

Identifiers

Catalog Number
717272 FDA UDI
Primary DI / UDI-DI
00050428371053 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

CVS Health by Woonsocket Prescription Center, Incorporated — 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

Sources (1)

  • FDA UDI 9a686aed-5eda-4364-9376-2f05fecf7a3f 37 fields · synced Jun 8, 2026