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Cardinal Health

FDA UDI

Class I (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
CARDINAL HEALTH FDA UDI
Generic Name
Skin-cover sealant FDA UDI
Device Name
Barrier Protectant No-Sting Wipe Alcohol Free Protects skin from: Incontinence Bodily fluids Adhesive stripping FDA UDI
Model / Reference
CSC-BNS-WP FDA UDI
Description
Barrier Protectant No-Sting Wipe Alcohol Free Protects skin from: Incontinence Bodily fluids Adhesive stripping FDA UDI

Identifiers

Catalog Number
CSC-BNS-WP FDA UDI
Primary DI / UDI-DI
00885380049111 FDA UDI
FDA Product Code
NEC FDA UDI
GMDN Term
Skin-cover sealant FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5090 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Skin-cover sealant

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

Similar devices

Also classified as Skin-cover sealant.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d0292d3a-1688-43a8-855a-f4b0ba20cf92 34 fields · synced Jun 8, 2026