MONICA NOVII WIRELESS PATCH SYSTEM 107-PT-001-1

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2019-11-12 for MONICA NOVII WIRELESS PATCH SYSTEM 107-PT-001-1 manufactured by Monica Healthcare Ltd.

MAUDE Entry Details

Report Number3006340424-2019-00002
MDR Report Key9309369
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2019-11-12
Date of Report2019-11-12
Date of Event2019-10-05
Date Mfgr Received2019-10-22
Device Manufacturer Date2018-10-09
Date Added to Maude2019-11-12
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 ContactJOHN SZALINSKI
Manufacturer Street3000 N GRANDVIEW BLVD.
Manufacturer CityWAUKESHA WI
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMONICA NOVII WIRELESS PATCH SYSTEM
Generic NameUTERINE ELECTROMYOGRAPHIC MONITOR
Product CodeOSP
Date Received2019-11-12
Model Number107-PT-001-1
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerMONICA HEALTHCARE LTD
Manufacturer AddressUNIT 8, INTERCHANGE 25 BUSINESS PARK BOSTOCKS LANE NOTTINGHAM NG105QG UK NG10 5QG


Patients

Patient NumberTreatmentOutcomeDate
10 2019-11-12

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