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Men's Liberty

FDA UDI

Class I (US FDA UDI)

by Argentum Medical, Llc

Identity

Trade Name
Men's Liberty FDA UDI
Generic Name
Penis wearable urinal FDA UDI
Device Name
Men's Liberty (30 per box), Canada FDA UDI
Model / Reference
23046-30CA FDA UDI
Description
Men's Liberty (30 per box), Canada FDA UDI

Identifiers

Primary DI / UDI-DI
00653599002162 FDA UDI
FDA Product Code
NOA FDA UDI
GMDN Term
Penis wearable urinal FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.5250 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Penis wearable urinal

Men's Liberty by Argentum Medical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Penis wearable urinal.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Argentum Medical, Llc

Sources (1)

  • FDA UDI ce366f2f-e37e-4f7b-a5f4-dcb8fea05c53 35 fields · synced Jun 1, 2026