TUBING, PUMP, CARDIOPULMONARY BYPASS VKMO 71000 70106.7949

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-02-13 for TUBING, PUMP, CARDIOPULMONARY BYPASS VKMO 71000 70106.7949 manufactured by Maquet Cardiopulmonary Gmbh.

MAUDE Entry Details

Report Number8010762-2020-00057
MDR Report Key9705287
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-02-13
Date of Report2020-03-30
Date of Event2020-01-28
Date Mfgr Received2020-03-30
Device Manufacturer Date2019-07-08
Date Added to Maude2020-02-13
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 StreetMAQUET CARDIOPULMONARY AG KEHLER STRASSE 31
Manufacturer CityRASTATT 76437
Manufacturer CountryGM
Manufacturer Postal76437
Manufacturer Phone4972229321
Manufacturer G1NURSEL BOELENS
Manufacturer StreetMAQUET CARDIOPULMONARY AG KEHLER STRASSE 31
Manufacturer CityRASTATT 76437
Manufacturer CountryGM
Manufacturer Postal Code76437
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTUBING, PUMP, CARDIOPULMONARY BYPASS
Generic NameTUBING, PUMP, CARDIOPULMONARY BYPASS
Product CodeDWE
Date Received2020-02-13
Returned To Mfg2020-03-02
Model NumberVKMO 71000
Catalog Number70106.7949
Lot Number92284996
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerMAQUET CARDIOPULMONARY GMBH
Manufacturer AddressNEUE ROTTENBURGER STRASSE 37 HECHINGEN US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-13

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