ROSCOE RMI-15MINI

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-10-03 for ROSCOE RMI-15MINI manufactured by Danyang Xinya Valve Co., Ltd.

MAUDE Entry Details

Report Number3012316249-2019-00028
MDR Report Key9152520
Date Received2019-10-03
Date of Report2019-10-03
Date Facility Aware2019-09-13
Report Date2019-10-03
Date Reported to FDA2019-10-03
Date Reported to Mfgr2019-10-03
Date Added to Maude2019-10-03
Event Key0
Report Source CodeDistributor report
Manufacturer LinkN
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 NameROSCOE
Generic NameREGULATOR 0-15 LPM
Product CodeCAN
Date Received2019-10-03
Model NumberRMI-15MINI
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Age21 MO
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerDANYANG XINYA VALVE CO., LTD
Manufacturer AddressNO. 12 DONGJIN WEST ROAD YANLING TOWN DANYANG JIANGSU, CHINA 212341 CH 212341


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization 2019-10-03

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