PORTIO CONE ATTACHMENT UNKNOWN

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,user f report with the FDA on 2020-03-18 for PORTIO CONE ATTACHMENT UNKNOWN manufactured by Richard Wolf Medical Instruments Corp..

MAUDE Entry Details

Report Number1418479-2020-00008
MDR Report Key9851346
Report SourceCOMPANY REPRESENTATIVE,USER F
Date Received2020-03-18
Date of Report2020-02-18
Date of Event2020-02-11
Date Mfgr Received2020-02-18
Date Added to Maude2020-03-18
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. DAISY RAMOS
Manufacturer Street353 CORPORATE WOODS PARKWAY
Manufacturer CityVERNON HILLS, IL
Manufacturer CountryUS
Manufacturer Phone9131113227
Manufacturer G1RICHARD WOLF MEDICAL INSTRUMENTS CORP.
Manufacturer Street353 CORPORATE WOODS PARKWAY
Manufacturer CityVERNON HILLS, IL
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePORTIO CONE ATTACHMENT
Generic NamePORTIO CONE ATTACHMENT
Product CodeHDC
Date Received2020-03-18
Model NumberUNKNOWN
Catalog NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerRICHARD WOLF MEDICAL INSTRUMENTS CORP.
Manufacturer Address353 CORPORATE WOODS PARKWAY VERNON HILLS, IL US


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization 2020-03-18

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