IRIS URETERAL KIT 0220180518

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2017-04-07 for IRIS URETERAL KIT 0220180518 manufactured by Stryker Endoscopy-san Jose.

Event Text Entries

[72116267] Additional information will be provided once the investigation has been completed. The device manufacture date is not known at this time. However, should it become available it will be provided in future reports. (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[72116268] It was reported that the patient was unable to pass urine normally due to the swelling of the ureters, requiring an additional medical procedure. The procedure was completed successfully.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number0002936485-2017-00354
MDR Report Key6472340
Report SourceHEALTH PROFESSIONAL
Date Received2017-04-07
Date of Report2017-07-20
Date of Event2017-03-15
Date Mfgr Received2017-03-16
Date Added to Maude2017-04-07
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. SANDHYA JAISHANKAR
Manufacturer Street5900 OPTICAL COURT
Manufacturer CitySAN JOSE CA 95138
Manufacturer CountryUS
Manufacturer Postal95138
Manufacturer Phone4087542000
Manufacturer G1STRYKER ENDOSCOPY-SAN JOSE
Manufacturer Street5900 OPTICAL COURT
Manufacturer CitySAN JOSE CA 95138
Manufacturer CountryUS
Manufacturer Postal Code95138
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameIRIS URETERAL KIT
Generic NameLIGHT, CATHETER, FIBEROPTIC, GLASS, URETERAL
Product CodeFCS
Date Received2017-04-07
Catalog Number0220180518
Lot NumberUNKNOWN
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER ENDOSCOPY-SAN JOSE
Manufacturer Address5900 OPTICAL COURT SAN JOSE CA 95138 US 95138


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2017-04-07

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