ANALYZER SURGICAL CABLE 2292

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2020-03-26 for ANALYZER SURGICAL CABLE 2292 manufactured by Cov Lp/llc, Augusta.

MAUDE Entry Details

Report Number1018120-2020-00002
MDR Report Key9884098
Report SourceCOMPANY REPRESENTATIVE
Date Received2020-03-26
Date of Report2020-03-26
Date of Event2020-02-10
Date Mfgr Received2020-03-25
Device Manufacturer Date2017-02-21
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 ContactPAULA BIXBY
Manufacturer Street8200 CORAL SEA ST NE
Manufacturer CityMOUNDS VIEW MN 55112
Manufacturer CountryUS
Manufacturer Postal55112
Manufacturer Phone7635055378
Manufacturer G1COV LP/LLC, AUGUSTA
Manufacturer Street1647 PERKINS RD
Manufacturer CityAUGUSTA GA 30913
Manufacturer CountryUS
Manufacturer Postal Code30913
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameANALYZER SURGICAL CABLE
Generic NamePROGRAMMER, PACEMAKER
Product CodeKRG
Date Received2020-03-26
Returned To Mfg2020-02-27
Model Number2292
Catalog Number2292
Lot Number2292
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerCOV LP/LLC, AUGUSTA
Manufacturer Address1647 PERKINS RD AUGUSTA GA 30913 US 30913


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-26

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