PULSE GEN MODEL 105

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 2020-01-24 for PULSE GEN MODEL 105 manufactured by Livanova Usa, Inc..

Event Text Entries

[183933293] Patient reported that they believe their device is depleted as they are having an increase in depression. No other relevant information has been received to date.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1644487-2020-00112
MDR Report Key9627922
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-01-24
Date of Report2020-02-18
Date of Event2019-11-29
Date Mfgr Received2020-01-24
Device Manufacturer Date2015-02-09
Date Added to Maude2020-01-24
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 ContactMRS. RACHEL KOHN
Manufacturer Street100 CYBERONICS BLVD SUITE 600
Manufacturer CityHOUSTON TX 77058
Manufacturer CountryUS
Manufacturer Postal77058
Manufacturer Phone2812287200
Manufacturer G1LIVANOVA USA, INC.
Manufacturer Street100 CYBERONICS BLVD SUITE 600
Manufacturer CityHOUSTON TX 77058
Manufacturer CountryUS
Manufacturer Postal Code77058
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePULSE GEN MODEL 105
Generic NameGENERATOR
Product CodeMUZ
Date Received2020-01-24
Model Number105
Lot Number203263
Device Expiration Date2017-01-20
OperatorLAY USER/PATIENT
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerLIVANOVA USA, INC.
Manufacturer Address100 CYBERONICS BLVD HOUSTON TX 77058 US 77058


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-24

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.