Walgreens

FDA UDI

Class I (US FDA UDI)

by Walgreen Co.

Identity

Trade Name: Walgreens FDA UDI
Generic Name: Menstrual pad, unscented FDA UDI
Device Name: MAXIPAD OVERNIGHT W/WINGS UNSCENTED 14CNT FDA UDI
Model / Reference: 170293 FDA UDI
Description: MAXIPAD OVERNIGHT W/WINGS UNSCENTED 14CNT FDA UDI

Identifiers

Primary DI / UDI-DI: 00049022633025 FDA UDI
FDA Product Code: HHD FDA UDI
GMDN Term: Menstrual pad, unscented FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 884.5435 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

Yes

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, unscented

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 93c59b19-f564-4618-9b25-694eaf77ffed 34 fields · synced May 31, 2026