EXABALTE 4000 SYS004000

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 SYS004000 manufactured by Insightec Ltd.

Event Text Entries

[142878489] The system technical performance during treatment was thoroughly reviewed; no technical issues were found. No system malfunction occurred.
Patient Sequence No: 1, Text Type: N, H10


[142878490] On (b)(6) 2018, insightec was notified, that patient who was treated on (b)(6) 2018, reported of numbness on the right side of the lips and in the first and second digits of the right hand following treatment for essential tremor. The patient also showed some balance issues. On (b)(6) 2018, the team had a phone call with the patient in which the patient reported that balance and numbness symptoms are improving, and the patient takes medrol dose pack. Further information will be available after patient will come for 3 months follow up visit.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9615058-2018-00009
MDR Report Key8543379
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2019-04-24
Date of Report2018-12-09
Date of Event2018-10-30
Date Mfgr Received2018-11-10
Device Manufacturer Date2013-03-21
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 NumberSYS004000
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. Deathisabilit 2019-04-24

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