VENOUS HARDSHELL CARDIOTOMY RESERVOIRS HQV 13122#QUADROX MEMBRANE SET 70104.6406

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-07-12 for VENOUS HARDSHELL CARDIOTOMY RESERVOIRS HQV 13122#QUADROX MEMBRANE SET 70104.6406 manufactured by Maquet Cardiopulmonary Gmbh.

MAUDE Entry Details

Report Number8010762-2019-00206
MDR Report Key8784136
Date Received2019-07-12
Date of Report2019-10-22
Date of Event2019-06-27
Date Mfgr Received2019-10-21
Device Manufacturer Date2018-11-23
Date Added to Maude2019-07-12
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 NameVENOUS HARDSHELL CARDIOTOMY RESERVOIRS
Generic NameRESERVOIR, BLOOD, CARDIOPULMONARY BYPASS
Product CodeDTN
Date Received2019-07-12
Returned To Mfg2019-08-01
Model NumberHQV 13122#QUADROX MEMBRANE SET
Catalog Number70104.6406
Lot Number92252156
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 2019-07-12

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