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Walgreens

FDA UDI

Class I (US FDA UDI)

by Walgreen Co.

Identity

Trade Name
Walgreens FDA UDI
Generic Name
Hand-held urinal, single-use FDA UDI
Device Name
MALE URINAL, 1000ML FDA UDI
Model / Reference
276743 FDA UDI
Description
MALE URINAL, 1000ML FDA UDI

Identifiers

Catalog Number
WRX276743 FDA UDI
Primary DI / UDI-DI
00311917158952 FDA UDI
FDA Product Code
FNP FDA UDI
GMDN Term
Hand-held urinal, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6730 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

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

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 1000 Milliliter FDA UDI

Category: Hand-held urinal, single-use

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

Similar devices

Also classified as Hand-held urinal, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Walgreen Co.

Sources (1)

  • FDA UDI b0c17c7c-7308-4f77-a488-a5f17aab1771 36 fields · synced Jun 8, 2026