A Plus

FDA UDI

Class U (US FDA UDI)

by A Plus International, Inc

Identity

Trade Name: A Plus FDA UDI
Generic Name: Non-woven gauze pad FDA UDI
Device Name: 4"X4", 3Ply, 200 Pc(s)/Bag, 20 Bags/Case, 4000 Pc(s)/Case FDA UDI
Model / Reference: 1 FDA UDI
Description: 4"X4", 3Ply, 200 Pc(s)/Bag, 20 Bags/Case, 4000 Pc(s)/Case FDA UDI

Identifiers

Catalog Number: NG-4403-3 FDA UDI
Primary DI / UDI-DI: 00683534850145 FDA UDI
FDA Product Code: EFQ FDA UDI
GMDN Term: Non-woven gauze pad FDA UDI

Classification

Device Class: U 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

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: Non-woven gauze pad

A Plus by A Plus International, Inc — Class U — 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 U	Pending data

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Manufacturer

Manufacturer: A Plus International, Inc

Sources (1)

FDA UDI 456860c8-3bcb-4527-9ecd-687f7e767b5a 34 fields · synced May 31, 2026