INFRAVISION URETERAL KIT 0220180516

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 07 report with the FDA on 2011-05-09 for INFRAVISION URETERAL KIT 0220180516 manufactured by Stryker Endoscopy San Jose.

Event Text Entries

[2078847] It was reported that during a laparoscopic procedure, the unit was not very visible through the wall of the urethra. It was further reported by the surgeon that he normally has a better view and the entire urethra is lit up.
Patient Sequence No: 1, Text Type: D, B5


[9014482] Add'l info will be provided once the investigation is completed.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2936485-2011-00300
MDR Report Key2133222
Report Source07
Date Received2011-05-09
Date of Report2011-04-11
Date of Event2011-04-11
Date Mfgr Received2011-04-11
Date Added to Maude2012-02-07
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 FDA0
Event Location0
Manufacturer ContactSUNNY OFFORJEBE
Manufacturer Street5900 OPTICAL CT.
Manufacturer CitySAN JOSE CA 95138
Manufacturer CountryUS
Manufacturer Postal95138
Manufacturer Phone4087542000
Manufacturer G1STRYKER ENDOSCOPY SAN JOSE
Manufacturer Street5900 OPTICAL CT.
Manufacturer CitySAN JOSE CA 95138
Manufacturer CountryUS
Manufacturer Postal Code95138
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameINFRAVISION URETERAL KIT
Generic NameCATHETER
Product CodeFAT
Date Received2011-05-09
Returned To Mfg2011-05-05
Catalog Number0220180516
Lot NumberPSTR091609-1
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER ENDOSCOPY SAN JOSE
Manufacturer AddressSAN JOSE CA 95138 US 95138


Patients

Patient NumberTreatmentOutcomeDate
10 2011-05-09

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