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ProACT Adjustable Continence Therapy for Men – 14 cm Single Implant - Revision 800022-14

by Uromedica Inc

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00180668000403 UDI-DI Date15 Jul 2016ListedStatusListed 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  • Withdrawn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
ProACT Adjustable Continence Therapy for Men – 14 cm Single Implant - Revision
Generic Name
Hydraulic male urinary incontinence treatment system
Model / Reference
800022-14
Primary DI / UDI-DI
00180668000403
GMDN Term
Hydraulic male urinary incontinence treatment system
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Conditional

Related devices

Category: Hydraulic male urinary incontinence treatment system

Other devices from Uromedica Inc

See all devices from Uromedica Inc →

Properties

  • Sterile
  • Single Use
  • Implantable
  • Convenience Kit
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

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