HLS SET ADVANCED 7.0 WITH BIOLINE COATING BEQ-HLS 7050 USA#HLS SET ADVANCED 7.0 701052794

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer,health professional, report with the FDA on 2020-02-17 for HLS SET ADVANCED 7.0 WITH BIOLINE COATING BEQ-HLS 7050 USA#HLS SET ADVANCED 7.0 701052794 manufactured by .

MAUDE Entry Details

Report Number8010762-2020-00066
MDR Report Key9717058
Report SourceCONSUMER,HEALTH PROFESSIONAL,
Date Received2020-02-17
Date of Report2020-04-01
Date of Event2020-02-10
Date Mfgr Received2020-03-25
Device Manufacturer Date2019-11-21
Date Added to Maude2020-02-17
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 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 NameHLS SET ADVANCED 7.0 WITH BIOLINE COATING
Generic NameOXYGENATOR, CARDIOPULMONARY BYPASS
Product CodeDTZ
Date Received2020-02-17
Model NumberBEQ-HLS 7050 USA#HLS SET ADVANCED 7.0
Catalog Number701052794
Lot Number70136151
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-17

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