Identity
- Trade Name
- DeRoyal FDA UDI
- Generic Name
- Negative-pressure wound therapy system dressing set FDA UDI
- Device Name
- Lifebridge NPWT Transition Kit FDA UDI
- Model / Reference
- NP-7DAYKITLB FDA UDI
- Description
- Lifebridge NPWT Transition Kit FDA UDI
Identifiers
- Catalog Number
- NP-7DAYKITLB FDA UDI
- Primary DI / UDI-DI
- 00749756351584 FDA UDI
- FDA Product Code
- KDD FDA UDI
- GMDN Term
- Negative-pressure wound therapy system dressing set FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
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
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: Negative-pressure wound therapy system dressing set
DeRoyal by Deroyal Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- AVELLE — CONVATEC, PURCHASING DEPARTMENT · Class II
- Solventum US LLC — KCI USA, INC. · Class II
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
- Deroyal Industries, Inc.
Sources (1)
- FDA UDI d8a4aa37-7aeb-4d08-9b2b-8d343aba3cf5 34 fields · synced Jun 8, 2026