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Walgreens

FDA UDI

Class II (US FDA UDI)

by Walgreen Co.

Identity

Trade Name
Walgreens FDA UDI
Generic Name
Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical FDA UDI
Device Name
Digital Wide-Tip & One Step Pregnancy Tests: A convenience kit consisting of 1 Digital Wide-Tip Pregnancy Test and 1 One Step Pregnancy Test FDA UDI
Model / Reference
733603 FDA UDI
Description
Digital Wide-Tip & One Step Pregnancy Tests: A convenience kit consisting of 1 Digital Wide-Tip Pregnancy Test and 1 One Step Pregnancy Test FDA UDI

Identifiers

Catalog Number
N/A FDA UDI
Primary DI / UDI-DI
00311917055589 FDA UDI
510(k) Number
K042280 FDA UDI
K060128 FDA UDI
FDA Product Code
LCX FDA UDI
GMDN Term
Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1155 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

Yes

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical

Walgreens by Walgreen Co. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Walgreen Co.

Sources (1)

  • FDA UDI e9d6eef8-9a1b-443c-b192-64493885ca00 37 fields · synced May 30, 2026