REGARD CORONARY RADIAL HT0952A 800747001

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-08-30 for REGARD CORONARY RADIAL HT0952A 800747001 manufactured by Resource Optimization & Innovation, L.l.c..

MAUDE Entry Details

Report Number8949525
MDR Report Key8949525
Date Received2019-08-30
Date of Report2019-08-22
Date of Event2019-01-30
Report Date2019-08-22
Date Reported to FDA2019-08-22
Date Reported to Mfgr2019-08-30
Date Added to Maude2019-08-30
Event Key0
Report Source CodeUser Facility report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameREGARD CORONARY RADIAL
Generic NameCARDIAC CATHETERIZATION KIT
Product CodeOES
Date Received2019-08-30
Model NumberHT0952A
Catalog Number800747001
Lot Number63704A
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerRESOURCE OPTIMIZATION & INNOVATION, L.L.C.
Manufacturer Address3000 E SAWYER RD REPUBLIC MO 65738 US 65738


Patients

Patient NumberTreatmentOutcomeDate
10 2019-08-30

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