HORIZON

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-02-13 for HORIZON manufactured by The Magstim Company Limited.

MAUDE Entry Details

Report Number3011755356-2020-00001
MDR Report Key9705314
Date Received2020-02-13
Date of Report2020-01-15
Date Facility Aware2020-01-15
Date Mfgr Received2020-01-15
Date Added to Maude2020-02-13
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
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameHORIZON
Generic NameHORIZON
Product CodeOBP
Date Received2020-02-13
Device AvailabilityY
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerTHE MAGSTIM COMPANY LIMITED
Manufacturer AddressSPRING GARDENS WHITLAND, SA340HR UK SA34 0HR


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-02-13

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