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RevivaSil Gel Pad Kit

FDA UDI

by Trifluent Pharma, LLC

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

Similar devices

Also classified as Scar-management dressing, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2538f7e8-1e73-4190-87b4-17b0f6bc370b 33 fields · synced May 30, 2026