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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: AXONICS, INC BULKAMID URETHRAL BULKING SYSTEM; AGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE

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AXONICS, INC BULKAMID URETHRAL BULKING SYSTEM; AGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE Back to Search Results
Model Number 50050
Medical Device Problem Code Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes Urinary Tract Infection (2120); Urinary Incontinence (4572)
Type of Reportable Event Serious Injury
Event or Problem Description
The patient experienced urinary tract infection and urinary incontinence.
 
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Brand Name
BULKAMID URETHRAL BULKING SYSTEM
Common Device Name
AGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE
Manufacturer (Section D)
AXONICS, INC
26 technology dr
irvine CA 92618
Manufacturer (Section G)
CONTURA INTERNATIONA A/S
23 sydmarken
soeborg
DK  
Manufacturer Contact
linda phan
26 technology drive
irvine, CA 92618
MDR Report Key19101581
Report Number3002968685-2024-00068
Device Sequence Number17977889
Product Code LNM
UDI-Device Identifier10810005340509
UDI-Public10810005340509
Combination Product (Y/N)N
Initial Reporter CountryUS
PMA/510(K) Number
P170023
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2023
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source Company Representative
Initial Reporter Occupation Other
Type of Report Initial
Report Date (Section B) 04/12/2024
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Model Number50050
Was Device Available for Evaluation? No
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 03/20/2024
Initial Report FDA Received Date04/12/2024
Was Device Evaluated by Manufacturer? (Y/N) Device Not Returned to Manufacturer
Is the Device Labeled for Single Use? (Y/N) Yes
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Usage of Device Initial
Patient Sequence Number1
Patient Age74 YR
Patient SexFemale
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