Walgreens

FDA UDI

Class I (US FDA UDI)

by Walgreen Co.

Identity

Trade Name: Walgreens FDA UDI
Generic Name: Menstrual pad, scented FDA UDI
Device Name: ULTRA THIN MAXIPAD LONG W/WINGS SUPER SCENTED 14CNT FDA UDI
Model / Reference: 901365 FDA UDI
Description: ULTRA THIN MAXIPAD LONG W/WINGS SUPER SCENTED 14CNT FDA UDI

Identifiers

Primary DI / UDI-DI: 00049022837515 FDA UDI
FDA Product Code: NRC FDA UDI
GMDN Term: Menstrual pad, scented FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 884.5425 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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Menstrual pad, scented

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 413d0286-4348-4287-b3f9-53eb9c419ab6 34 fields · synced May 30, 2026