Identity
- Trade Name
- CARDINAL HEALTH FDA UDI
- Generic Name
- Synthetic-polymer liquid barrier dressing FDA UDI
- Device Name
- Protective Barrier Wipe Protects skin for Adhesives, Incontinence, and Bodily Fluids Non-irritating to Intact Skin Thick, Soft Application Pad Instructions: Apply to clean, dry skin. Allow to air dry. Do not use on open wounds. Warning: For external use only. Single use only. Do not use with electrocautery procedures. Stinging may result from contact. Not made with natural rubber latex. Ingredients: Isopropyl alcohol, water, ethyl ester of PVM/MA copolymer, ethyl alcohol, acetyl tributyl citrate FDA UDI
- Model / Reference
- ZA40075 FDA UDI
- Description
- Protective Barrier Wipe Protects skin for Adhesives, Incontinence, and Bodily Fluids Non-irritating to Intact Skin Thick, Soft Application Pad Instructions: Apply to clean, dry skin. Allow to air dry. Do not use on open wounds. Warning: For external use only. Single use only. Do not use with electrocautery procedures. Stinging may result from contact. Not made with natural rubber latex. Ingredients: Isopropyl alcohol, water, ethyl ester of PVM/MA copolymer, ethyl alcohol, acetyl tributyl citrate FDA UDI
Identifiers
- Catalog Number
- ZA40075 FDA UDI
- Primary DI / UDI-DI
- 20885380182850 FDA UDI
- FDA Product Code
- KOX FDA UDI
- GMDN Term
- Synthetic-polymer liquid barrier dressing FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4730 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
MR Safe FDA UDI
Category: Synthetic-polymer liquid barrier dressing
Cardinal Health by Cardinal Health 200, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Synthetic-polymer liquid barrier dressing.
- Provox Wipes — ATOS MEDICAL INC. · Class I
- James Alexander Dispensing solution — JAMES ALEXANDER CORP. · Class I
- 3M™ Cavilon™ — 3M COMPANY · Class I
- 3M™ Steri-Strip™ — 3M COMPANY · Class I
- SECURA No-Sting Barrier Film Wipes Bulk — Smith & Nephew Medical, Ltd. · Class I
- Sting Free — DERMARITE INDUSTRIES LLC · Class I
- 3M™ Cavilon™ — 3M COMPANY · Class I
- ProCure — Twin Med, LLC · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Cardinal Health 200, LLC
Sources (1)
- FDA UDI be13f341-161e-469d-b6df-4b7d777fdf85 34 fields · synced Jun 8, 2026