Walgreens

FDA UDI

Class I (US FDA UDI)

by Walgreen Co.

Identity

Trade Name: Walgreens FDA UDI
Generic Name: Non-woven gauze pad FDA UDI
Device Name: Walgreens Rolled Gauze. 4 in X 2.5 yd. FDA UDI
Model / Reference: 150573 FDA UDI
Description: Walgreens Rolled Gauze. 4 in X 2.5 yd. FDA UDI

Identifiers

Catalog Number: WRX150573V1 FDA UDI
Primary DI / UDI-DI: 00311917141114 FDA UDI
FDA Product Code: NAB FDA UDI
GMDN Term: Non-woven gauze pad 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

Yes

FDA UDI

Single Use

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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Width — 4 Inch FDA UDI
Length — 2.5 Yard FDA UDI

Category: Non-woven gauze pad

Walgreens by Walgreen Co. — 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: Walgreen Co.

Sources (1)

FDA UDI 384f77fa-2f0e-4e3f-ba1e-04c97ed5b3a7 36 fields · synced May 30, 2026