Identity
- Trade Name
- 3M™ Veraflo™ FDA UDI
- Generic Name
- Irrigation negative-pressure wound therapy dressing FDA UDI
- Device Name
- 3M™ V.A.C. Veraflo Cleanse™ Dressing, ULTVCL05MD, Medium, Cavilon Warning Label, 5/CS FDA UDI
- Model / Reference
- ULTVCL05MD FDA UDI
- Description
- 3M™ V.A.C. Veraflo Cleanse™ Dressing, ULTVCL05MD, Medium, Cavilon Warning Label, 5/CS FDA UDI
Identifiers
- Catalog Number
- ULTVCL05MD FDA UDI
- Primary DI / UDI-DI
- 10849554014029 FDA UDI
- FDA Product Code
- OMP FDA UDI
- GMDN Term
- Irrigation negative-pressure wound therapy dressing FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4780 FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
Combination Product
No
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Conditional FDA UDI
3M™ Veraflo™ by Kci Usa, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 II | Pending data |
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Manufacturer
- Manufacturer
- Kci Usa, Inc.
Sources (1)
- FDA UDI 5cee6cdb-ba1a-40d9-9b08-3d4edbad8952 36 fields · synced Jun 1, 2026