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SilDerm Scar Spray

FDA UDI

Class I (US FDA UDI)

by Skingen Uk Ltd

Identity

Trade Name
SilDerm Scar Spray FDA UDI
Generic Name
Scar-management dressing, reusable FDA UDI
Device Name
Silicone Scar Spray in bottles made from zylinderfl.60, glasklar PETG, 5g, M300 smooth white Spray head. Label material white PP with UV gloss varnish FDA UDI
Model / Reference
60ml FDA UDI
Description
Silicone Scar Spray in bottles made from zylinderfl.60, glasklar PETG, 5g, M300 smooth white Spray head. Label material white PP with UV gloss varnish FDA UDI

Identifiers

Catalog Number
SDSCR60 FDA UDI
Primary DI / UDI-DI
15060295490100 FDA UDI
FDA Product Code
MDA FDA UDI
GMDN Term
Scar-management dressing, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4025 FDA UDI
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

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

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: Scar-management dressing, reusable

SilDerm Scar Spray by Skingen Uk Ltd — Class I — 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

Manufacturer
Skingen Uk Ltd

Sources (1)

  • FDA UDI 28d2748b-f7e2-44f3-99d1-df938dd73853 35 fields · synced Jun 1, 2026