E-POLY 36MM +3 MAXROM LNR SZ23 N/A EP-108223

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 2019-06-10 for E-POLY 36MM +3 MAXROM LNR SZ23 N/A EP-108223 manufactured by Zimmer Biomet, Inc..

MAUDE Entry Details

Report Number0001825034-2019-02495
MDR Report Key8682334
Report SourceDISTRIBUTOR,HEALTH PROFESSION
Date Received2019-06-10
Date of Report2019-08-27
Date of Event2019-05-21
Date Mfgr Received2019-08-26
Device Manufacturer Date2015-01-06
Date Added to Maude2019-06-10
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
Removal Correction NumberN/A
Event Type3
Type of Report3

Device Details

Brand NameE-POLY 36MM +3 MAXROM LNR SZ23
Generic NameHIP PROSTHESIS
Product CodeMAY
Date Received2019-06-10
Returned To Mfg2019-06-10
Model NumberN/A
Catalog NumberEP-108223
Lot Number841250
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerZIMMER BIOMET, INC.
Manufacturer Address56 E. BELL DRIVE WARSAW IN 46582 US 46582


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Required No Informationntervention 2019-06-10

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