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SiliGentle Silicone Bordered Foam Dressing

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
SiliGentle Silicone Bordered Foam Dressing FDA UDI
Generic Name
Pressure-management bandage, silicone FDA UDI
Device Name
SiliGentle Silicone Bordered Foam Dressing, 4"x4" FDA UDI
Model / Reference
3059 FDA UDI
Description
SiliGentle Silicone Bordered Foam Dressing, 4"x4" FDA UDI

Identifiers

Primary DI / UDI-DI
00616784305912 FDA UDI
FDA Product Code
NAD FDA UDI
GMDN Term
Pressure-management bandage, silicone FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4020 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

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: Pressure-management bandage, silicone

SiliGentle Silicone Bordered Foam Dressing by Dynarex Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pressure-management bandage, silicone.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI 5952a090-904d-46be-997e-b403ab2130ce 33 fields · synced May 30, 2026