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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
PANTILINER REGULAR THIN UNSCENTED 120CNT FDA UDI
Model / Reference
603012 FDA UDI
Description
PANTILINER REGULAR THIN UNSCENTED 120CNT FDA UDI

Identifiers

Primary DI / UDI-DI
00049022562059 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

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

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

Similar devices

Also classified as Menstrual pad, unscented.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Walgreen Co.

Sources (1)

  • FDA UDI 5dbbb0ad-c723-468d-ab95-d00e20737d9d 34 fields · synced May 31, 2026