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Men's Liberty Acute MLAM

by Argentum Medical, LLC

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00653599002452 UDI-DI Date23 Jan 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Men's Liberty Acute
Generic Name
Urinary incontinence penis sheath/port, single-use
Model / Reference
MLAM
Primary DI / UDI-DI
00653599002452
FDA Product Code
NOA
GMDN Term
Urinary incontinence penis sheath/port, single-use
Device Class
Class I
Regulation Number
876.5250
GUDID distribution status
In Commercial Distribution

Other devices from Argentum Medical, LLC

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Properties

  • Single Use
  • Convenience Kit
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No