VISERA ELITE XENON LIGHT SOURCE CLV-S190

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2016-10-18 for VISERA ELITE XENON LIGHT SOURCE CLV-S190 manufactured by Olympus Medical Systems Corp..

Event Text Entries

[57692610] The subject device has not been returned to olympus for investigation yet. Olympus will investigate the subject device to determine the cause of this phenomenon after olympus receives it. Olympus will submit a supplemental mdr report after the cause of this phenomenon is found.
Patient Sequence No: 1, Text Type: N, H10


[57692611] During the laparoscopic cholecystectomy with the subject clv-s190, the cooling fan of the clv-s190 did not work and the emergency lamp started up. The user facility replaced the system including the subject clv-s190 to another system to complete the procedure. There was no report of the patient injury other than replacing the device.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number8010047-2016-01356
MDR Report Key6035886
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2016-10-18
Date of Report2016-10-18
Date of Event2016-09-21
Date Mfgr Received2016-09-21
Date Added to Maude2016-10-18
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. SUSUMU NISHINA
Manufacturer Street2951 ISHIKAWA-CHO
Manufacturer CityHACHIOJI-SH, TOKYO 192-8507
Manufacturer CountryJA
Manufacturer Postal192-8507
Manufacturer Phone42 6425177
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameVISERA ELITE XENON LIGHT SOURCE
Generic NameLIGHT SOURCE
Product CodeGCT
Date Received2016-10-18
Model NumberCLV-S190
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerOLYMPUS MEDICAL SYSTEMS CORP.
Manufacturer Address2951 ISHIKAWA-CHO HACHIOJI-SHI, TOKYO 192-8507 JA 192-8507


Patients

Patient NumberTreatmentOutcomeDate
10 2016-10-18

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