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Scaraway Silicone Gel 20g

FDA UDI

Class I (US FDA UDI)

by L Perrigo Company

Identity

Trade Name
SCARAWAY SILICONE GEL 20G FDA UDI
Generic Name
Scar-management dressing, single-use FDA UDI
Device Name
PC: 11A FDA UDI
Model / Reference
11A3QSAC1 FDA UDI
Description
PC: 11A FDA UDI

Identifiers

Primary DI / UDI-DI
00070030511739 FDA UDI
FDA Product Code
MDA FDA UDI
GMDN Term
Scar-management dressing, single-use 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

Yes

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Scar-management dressing, single-use

Scaraway Silicone Gel 20g by L Perrigo Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Scar-management dressing, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
L Perrigo Company

Sources (1)

  • FDA UDI aaa6dbab-0911-43d2-a9bb-5720bc5a9a5b 33 fields · synced Jun 6, 2026