First Aid Only

FDA UDI

Class I (US FDA UDI)

by Acme United Corp.

Identity

Trade Name: First Aid Only FDA UDI
Generic Name: Woven gauze roll, non-sterile FDA UDI
Device Name: 4"x4 yd Non-Sterile Conforming Gauze Roll 1/Box FDA UDI
Model / Reference: 51018-001 FDA UDI
Description: 4"x4 yd Non-Sterile Conforming Gauze Roll 1/Box FDA UDI

Identifiers

Catalog Number: 51018-001 FDA UDI
Primary DI / UDI-DI: 00073577510180 FDA UDI
FDA Product Code: NAB FDA UDI
GMDN Term: Woven gauze roll, non-sterile FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4014 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Woven gauze roll, non-sterile

First Aid Only by Acme United Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Acme United Corp.

Sources (1)

FDA UDI 0a07a43f-21e0-453b-9c77-518a5a3ba030 35 fields · synced Jun 20, 2026