TR BAND N/A UNK

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-03-04 for TR BAND N/A UNK manufactured by Terumo Medical Corporation.

MAUDE Entry Details

Report Number1118880-2020-00065
MDR Report Key9785675
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-03-04
Date of Report2020-03-04
Date of Event2020-02-10
Date Mfgr Received2020-03-18
Date Added to Maude2020-03-04
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
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
Manufacturer ContactTHERESA MUSSAW
Manufacturer Street950 ELKTON BLVD.
Manufacturer CityELKTON, MD
Manufacturer CountryUS
Manufacturer Phone2837866718
Manufacturer G1TERUMO MEDICAL CORPORATION
Manufacturer Street950 ELKTON BLVD.
Manufacturer CityELKTON, MD
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTR BAND
Generic NameCLAMP, VASCULAR
Product CodeDXC
Date Received2020-03-04
Model NumberN/A
Catalog NumberUNK
Lot NumberUNK
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerTERUMO MEDICAL CORPORATION
Manufacturer Address950 ELKTON BLVD. ELKTON, MD US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-04

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