EMPRINT CA15L1

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign,health pr report with the FDA on 2019-11-18 for EMPRINT CA15L1 manufactured by Covidien Medical Products.

MAUDE Entry Details

Report Number3006451981-2019-00232
MDR Report Key9339074
Report SourceDISTRIBUTOR,FOREIGN,HEALTH PR
Date Received2019-11-18
Date of Report2019-11-18
Date of Event2019-10-23
Date Mfgr Received2019-11-01
Device Manufacturer Date2019-07-02
Date Added to Maude2019-11-18
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 ContactAMY BEEMAN
Manufacturer Street161 CHESHIRE LANE, SUITE 100
Manufacturer CityPLYMOUTH MN 55441
Manufacturer CountryUS
Manufacturer Postal55441
Manufacturer Phone7632104064
Manufacturer G1COVIDIEN MEDICAL PRODUCTS
Manufacturer StreetBUILDING 10- NO 789 PUXING ROA
Manufacturer CitySHANGHAI 201114
Manufacturer CountryCN
Manufacturer Postal Code201114
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameEMPRINT
Generic NameSYSTEM, ABLATION, MICROWAVE AND ACCESSORIES
Product CodeNEY
Date Received2019-11-18
Returned To Mfg2019-11-11
Model NumberCA15L1
Catalog NumberCA15L1
Lot NumberS9GG002X
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerCOVIDIEN MEDICAL PRODUCTS
Manufacturer AddressBUILDING 10- NO 789 PUXING ROA SHANGHAI 201114 CN 201114


Patients

Patient NumberTreatmentOutcomeDate
10 2019-11-18

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