EXABLATE 4000

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a other report with the FDA on 2020-03-24 for EXABLATE 4000 manufactured by Insightec Ltd.

Event Text Entries

[187758643] The (b)(6) post could not be confirmed with the treating physician. Not enough details to locate the site or the specific treatment. Not enough details to investigate.
Patient Sequence No: 1, Text Type: N, H10


[187758644] This complaint was posted on insightec (b)(6) page. The patient stated that she had brain treatment for essential tremor 2 weeks ago (apparently on (b)(6) 2020) and since then she has "significant right side weakness". Based on the available information, the company has not enough details to locate the site or the treating physician. The complainant received a post back that she should reach her treating physician or contact insightec formal website. No further information was received regarding this case so far.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9615058-2020-00007
MDR Report Key9870842
Report SourceOTHER
Date Received2020-03-24
Date of Report2020-03-24
Date of Event2020-02-12
Date Mfgr Received2020-02-26
Date Added to Maude2020-03-24
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 ContactMS. MEITAL TRANK
Manufacturer Street5 NACHUM HETH STREET
Manufacturer CityTIRAT CARMEL, 39120
Manufacturer CountryIS
Manufacturer Postal39120
Manufacturer G1INSIGHTEC LTD
Manufacturer Street5 NACHUM HETH
Manufacturer CityTIRAT CARMEL, 39120
Manufacturer CountryIS
Manufacturer Postal Code39120
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameEXABLATE 4000
Generic NameMR GUIDED FOCUSED ULTRASOUND SYSTEM
Product CodePOH
Date Received2020-03-24
Model Number4000
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerINSIGHTEC LTD
Manufacturer Address5 NACHUM HETH STREET TIRAT CARMEL, 39120 IS 39120


Patients

Patient NumberTreatmentOutcomeDate
101. Deathisabilit 2020-03-24

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