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Sterile Bordered Gauze

FDA UDI

Class I (US FDA UDI)

by Dermarite Industries Llc

Identity

Trade Name
Sterile Bordered Gauze FDA UDI
Generic Name
Adhesive bandage FDA UDI
Model / Reference
11230 FDA UDI

Identifiers

Primary DI / UDI-DI
00714196390288 FDA UDI
FDA Product Code
NAC FDA UDI
GMDN Term
Adhesive bandage FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4018 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Adhesive bandage

Sterile Bordered Gauze by Dermarite Industries Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Adhesive bandage.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7e338551-8ec3-4abe-80c5-ffb313cbfdd1 32 fields · synced Jun 1, 2026