COBRA? FUSION? 150 ABLATION MINIMALLY INVASIVE SYSTEM COBRA FUSION 150 ABLATION MININALLY INVASIVE SYSTE 001-700-001MI

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 2020-01-08 for COBRA? FUSION? 150 ABLATION MINIMALLY INVASIVE SYSTEM COBRA FUSION 150 ABLATION MININALLY INVASIVE SYSTE 001-700-001MI manufactured by Atricure, Inc..

MAUDE Entry Details

Report Number3011706110-2020-00001
MDR Report Key9565271
Report SourceDISTRIBUTOR,FOREIGN,HEALTH PR
Date Received2020-01-08
Date of Report2020-01-08
Date of Event2019-11-12
Date Mfgr Received2019-12-09
Device Manufacturer Date2019-04-01
Date Added to Maude2020-01-08
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 ContactMR. JOHN EHLERT
Manufacturer Street7555 INNOVATION WAY
Manufacturer CityMASON OH 45040
Manufacturer CountryUS
Manufacturer Postal45040
Manufacturer Phone5136448220
Manufacturer G1ATRICURE, INC.
Manufacturer Street7555 INNOVATION WAY
Manufacturer CityMASON OH 45040
Manufacturer CountryUS
Manufacturer Postal Code45040
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCOBRA? FUSION? 150 ABLATION MINIMALLY INVASIVE SYSTEM
Generic NameCOBRA? FUSION? 150 ABLATION MINIMALLY INVASIVE SYSTEM
Product CodeOCL
Date Received2020-01-08
Returned To Mfg2019-12-09
Model NumberCOBRA FUSION 150 ABLATION MININALLY INVASIVE SYSTE
Catalog Number001-700-001MI
Lot Number92858
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerATRICURE, INC.
Manufacturer Address7555 INNOVATION WAY MASON OH 45040 US 45040


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-08

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