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

GUDID 00180668000403

UROMEDICA INC

Hydraulic male urinary incontinence treatment system
Primary Device ID00180668000403
NIH Device Record Keye5162b6c-98ae-40a2-a961-ac138c173637
Commercial Distribution StatusIn Commercial Distribution
Brand NameProACT Adjustable Continence Therapy for Men – 14 cm Single Implant - Revision
Version Model Number800022-14
Company DUNS080378479
Company NameUROMEDICA INC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100180668000403 [Primary]

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-01-23
Device Publish Date2016-07-15

Devices Manufactured by UROMEDICA INC

00180668000144 - ProACT - Replacement Actuator - Tissue Expanding Device II2019-10-31
00180668000106 - ProACT - Implantation Instrument Set2019-01-23
00180668000137 - ProACT - Blunt Trocar2019-01-23
00180668000205 - ProACT - Tissue Expanding Device II2019-01-23
00180668000236 - ProACT Adjustable Continence Therapy for Men – 12 cm Implants - Patient Pack2019-01-23
00180668000380 - ProACT Adjustable Continence Therapy for Men – 14 cm Implants - Patient Pack2019-01-23
00180668000397 - ProACT Adjustable Continence Therapy for Men – 12 cm Single Implant - Revision2019-01-23
00180668000403 - ProACT Adjustable Continence Therapy for Men – 14 cm Single Implant - Revision2019-01-23
00180668000403 - ProACT Adjustable Continence Therapy for Men – 14 cm Single Implant - Revision2019-01-23

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