MOTOR MR8 ELECTRIC EM800

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2020-03-26 for MOTOR MR8 ELECTRIC EM800 manufactured by Mdt Powered Surgical Solutions.

MAUDE Entry Details

Report Number1625507-2020-00037
MDR Report Key9883154
Report SourceFOREIGN,HEALTH PROFESSIONAL
Date Received2020-03-26
Date of Report2020-03-26
Date of Event2020-02-27
Date Mfgr Received2020-02-27
Device Manufacturer Date2019-08-23
Date Added to Maude2020-03-26
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 ContactSTACY RUEMPING
Manufacturer Street4620 NORTH BEACH STREET
Manufacturer CityFT. WORTH TX 761373291
Manufacturer CountryUS
Manufacturer Postal761373291
Manufacturer Phone7635260594
Manufacturer G1MDT POWERED SURGICAL SOLUTIONS
Manufacturer Street4620 N BEACH ST
Manufacturer CityFORT WORTH TX 76137
Manufacturer CountryUS
Manufacturer Postal Code76137
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMOTOR MR8 ELECTRIC
Generic NameMOTOR, DRILL, PNEUMATIC
Product CodeHBB
Date Received2020-03-26
Returned To Mfg2020-03-24
Model NumberEM800
Catalog NumberEM800
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerMDT POWERED SURGICAL SOLUTIONS
Manufacturer Address4620 N BEACH ST FORT WORTH TX 76137 US 76137


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-03-26

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