UROPASS AS 11/13FR X 46 CM 5/BX 61146BX

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-07-21 for UROPASS AS 11/13FR X 46 CM 5/BX 61146BX manufactured by Teleflex Medical Oem.

Event Text Entries

[80956427] Device not yet returned.
Patient Sequence No: 1, Text Type: N, H10


[80956428] Mhra - incident report states: ureteral access sheath was being inserted into right ureter by surgeon and it was noted that the end of catheter was split. A second ureteral sheath was used only to find that it split at the same point. Third ureteral sheath was used with same result.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3005975494-2017-00003
MDR Report Key6733905
Date Received2017-07-21
Date of Report2018-02-15
Date of Event2017-06-21
Date Mfgr Received2018-02-13
Date Added to Maude2017-07-21
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR TERRENCE SULLIVAN
Manufacturer Street136 TURNPIKE ROAD
Manufacturer CitySOUTHBOROUGH MA 01772
Manufacturer CountryUS
Manufacturer Postal01772
Manufacturer Phone508804-273
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameUROPASS AS 11/13FR X 46 CM 5/BX
Product CodeKNY
Date Received2017-07-21
Returned To Mfg2017-07-19
Model Number61146BX
Lot Number09E1600089
ID NumberUDI
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerTELEFLEX MEDICAL OEM
Manufacturer Address3750 ANNAPOLIS LANE NORTH, SUITE 160 PLYMOUTH MN 55447 US 55447


Patients

Patient NumberTreatmentOutcomeDate
10 2017-07-21

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