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Webcol

FDA UDI

Class U (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
Webcol FDA UDI
Generic Name
Skin cleaning wipe FDA UDI
Device Name
Skin Cleansing Alcohol Prep 2 ply Medium Saturated with 70% Isopropyl Alcohol FDA UDI
Model / Reference
6818-1 FDA UDI
Description
Skin Cleansing Alcohol Prep 2 ply Medium Saturated with 70% Isopropyl Alcohol FDA UDI

Identifiers

Catalog Number
6818-1 FDA UDI
Primary DI / UDI-DI
10192253047073 FDA UDI
FDA Product Code
LKB FDA UDI
GMDN Term
Skin cleaning wipe FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Skin cleaning wipe

Webcol by Cardinal Health 200, LLC — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin cleaning wipe.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a46e692c-665b-427e-b03e-368213f35599 34 fields · synced Jun 8, 2026