EZ PASS 70 DEGREE RIGHT NI 904053

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,health profession report with the FDA on 2019-12-31 for EZ PASS 70 DEGREE RIGHT NI 904053 manufactured by Zimmer Biomet, Inc..

MAUDE Entry Details

Report Number0001825034-2019-05794
MDR Report Key9535154
Report SourceDISTRIBUTOR,HEALTH PROFESSION
Date Received2019-12-31
Date of Report2020-03-20
Date of Event2019-12-03
Date Mfgr Received2020-03-16
Date Added to Maude2019-12-31
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. CHRISTINA ARNT
Manufacturer Street56 E. BELL DR.
Manufacturer CityWARSAW IN 46582
Manufacturer CountryUS
Manufacturer Postal46582
Manufacturer Phone5745273773
Manufacturer G1ZIMMER BIOMET, INC.
Manufacturer Street56 E. BELL DRIVE
Manufacturer CityWARSAW IN 46582
Manufacturer CountryUS
Manufacturer Postal Code46582
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameEZ PASS 70 DEGREE RIGHT
Generic NameORTHOPEDIC MANUAL SURGICAL INSTRUMENT
Product CodeHWQ
Date Received2019-12-31
Returned To Mfg2019-12-23
Model NumberNI
Catalog Number904053
Lot NumberNI
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerZIMMER BIOMET, INC.
Manufacturer Address56 E. BELL DRIVE WARSAW IN 46582 US 46582


Patients

Patient NumberTreatmentOutcomeDate
10 2019-12-31

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