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Men's Liberty Acute

FDA UDI

Class I (US FDA UDI)

by Argentum Medical, Llc

Identity

Trade Name
Men's Liberty Acute FDA UDI
Generic Name
Urinary incontinence penis sheath/port, single-use FDA UDI
Device Name
Men's Liberty Acute Compatible with Suction with CathGrip FDA UDI
Model / Reference
2102616 FDA UDI
Description
Men's Liberty Acute Compatible with Suction with CathGrip FDA UDI

Identifiers

Primary DI / UDI-DI
00653599001950 FDA UDI
FDA Product Code
NOA FDA UDI
GMDN Term
Urinary incontinence penis sheath/port, single-use 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: Urinary incontinence penis sheath/port, single-use

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

Similar devices

Also classified as Urinary incontinence penis sheath/port, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f24aa14e-edcb-45de-aa7b-7efe51e700ef 35 fields · synced Jun 8, 2026