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Webcol

FDA UDI

Class U (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Webcol FDA UDI
Generic Name
Skin-cleaning wipe, sterile FDA UDI
Device Name
Alcohol Prep,2 Ply, Medium FDA UDI
Model / Reference
6818 FDA UDI
Description
Alcohol Prep,2 Ply, Medium FDA UDI

Identifiers

Catalog Number
6818 FDA UDI
Primary DI / UDI-DI
20884527020642 FDA UDI
FDA Product Code
LKB FDA UDI
GMDN Term
Skin-cleaning wipe, sterile 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

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Skin-cleaning wipe, sterile

Webcol by Cardinalhealth — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin-cleaning wipe, sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 7832094a-4213-4d24-a173-e6480fbaa57b 36 fields · synced May 30, 2026