Identity
- Trade Name
- RevivaSil Gel Pad Kit FDA UDI
- Generic Name
- Scar-management dressing, reusable FDA UDI
- Device Name
- Kit. Including four scar management dressings, reusable. FDA UDI
- Model / Reference
- 01 FDA UDI
- Description
- Kit. Including four scar management dressings, reusable. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00373352540013 FDA UDI
- GMDN Term
- Scar-management dressing, reusable FDA UDI
Classification
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
Yes
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: Scar-management dressing, reusable
RevivaSil Gel Pad Kit by Trifluent Pharma, LLC — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Scar-management dressing, reusable.
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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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Trifluent Pharma, LLC
Sources (1)
- FDA UDI 2538f7e8-1e73-4190-87b4-17b0f6bc370b 33 fields · synced May 30, 2026