Identity
- Trade Name
- Xeroform FDA UDI
- Generic Name
- Wound-nonadherent dressing, permeable, non-antimicrobial FDA UDI
- Device Name
- Xeroform Occlusive Gauze Roll 3 percent Bismuth Tribromophenate in Petrolatum Blend 5 x 9 in. (12.7 x 22.9 cm) FDA UDI
- Model / Reference
- 8884433605 FDA UDI
- Description
- Xeroform Occlusive Gauze Roll 3 percent Bismuth Tribromophenate in Petrolatum Blend 5 x 9 in. (12.7 x 22.9 cm) FDA UDI
Identifiers
- Catalog Number
- 8884433605 FDA UDI
- Primary DI / UDI-DI
- 10192253047868 FDA UDI
- FDA Product Code
- FRO FDA UDI
- GMDN Term
- Wound-nonadherent dressing, permeable, non-antimicrobial 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
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
Yes
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Width — 12.7 Centimeter FDA UDILength — 22.9 Centimeter FDA UDI
Category: Wound-nonadherent dressing, permeable, non-antimicrobial
Xeroform by Cardinal Health 200, LLC — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 U | Pending data |
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Manufacturer
- Manufacturer
- Cardinal Health 200, LLC
Sources (1)
- FDA UDI 24ab0b6c-6c4f-42d8-9fc4-7fb354d30252 35 fields · synced Jun 8, 2026