Identity
- Trade Name
- CARDINAL HEALTH FDA UDI
- Generic Name
- Synthetic-polymer liquid barrier dressing FDA UDI
- Device Name
- Sting Free 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. Wipe the desired area of the skin in a smooth sweeping motion until the entire area has a uniform coating. Adhesives can be applied within 30 seconds of application. Re-apply the wipe each time dressing is changed or adhesive products are removed. Warning: For external use only. Single use only. Keep out of reach of children. Caution: DO NOT USE as the only protective covering in situations that require dressing protection from bacterial contamination or on infected areas of the skin. Not made with natural rubber latex. Ingredients: Water, Lipo PEG-55, Tomadol 25-9, DMDM Hydantoin, Glycerin FDA UDI
- Model / Reference
- ZA20075 FDA UDI
- Description
- Sting Free 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. Wipe the desired area of the skin in a smooth sweeping motion until the entire area has a uniform coating. Adhesives can be applied within 30 seconds of application. Re-apply the wipe each time dressing is changed or adhesive products are removed. Warning: For external use only. Single use only. Keep out of reach of children. Caution: DO NOT USE as the only protective covering in situations that require dressing protection from bacterial contamination or on infected areas of the skin. Not made with natural rubber latex. Ingredients: Water, Lipo PEG-55, Tomadol 25-9, DMDM Hydantoin, Glycerin FDA UDI
Identifiers
- Catalog Number
- ZA20075 FDA UDI
- Primary DI / UDI-DI
- 20885380182843 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
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Also classified as Synthetic-polymer liquid barrier dressing.
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- 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 de2d6ddd-c08c-464d-a7e2-31144165537f 34 fields · synced Jun 8, 2026