EXABALTE 4000 SYS940352

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2019-04-24 for EXABALTE 4000 SYS940352 manufactured by Insightec Ltd.

Event Text Entries

[142875231] The system technical performance during treatment was thoroughly reviewed;no technical issues were found. No system malfunction occurred. All sonication parameters were within the normal ranges with no exceptional usage.
Patient Sequence No: 1, Text Type: N, H10


[142875232] On (b)(6) 2018, insightec was notified, that patient who was treated on (b)(6) 2018 experienced mild right leg ataxia on the same day as his left thalamotomy for essential tremor. The physician reported an improvement on patient condition since the day of treatment, but the condition still present. No side effect has been observed during and after the treatment nor reported. The patient had significant tremor relief after the treatment. At this time, there is no additional information.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9615058-2018-00008
MDR Report Key8543362
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2019-04-24
Date of Report2018-11-06
Date of Event2018-09-26
Date Mfgr Received2018-10-06
Device Manufacturer Date2016-12-08
Date Added to Maude2019-04-24
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 IDAN COHEN
Manufacturer Street5 NACHUM HETH STREET
Manufacturer CityTIRAT CARMEL, 39120
Manufacturer CountryIS
Manufacturer Postal39120
Manufacturer G1INSIGHTEC LTD
Manufacturer Street5 NACHUM HETH STREET
Manufacturer CityTIRAT CARMEL, 39120
Manufacturer CountryIS
Manufacturer Postal Code39120
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameEXABALTE 4000
Generic NameMR GUIDED FOCUSED ULTRASOUND SYSTEM
Product CodePOH
Date Received2019-04-24
Model Number4000
Catalog NumberSYS940352
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerINSIGHTEC LTD
Manufacturer Address5 NACHUM HETH STREET TIRAT CARMEL, 39120 IS 39120


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Deathisabilit 2019-04-24

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