COMPRESSOR MINI COMPR MINI 230V 50HZ 6481787

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-10-28 for COMPRESSOR MINI COMPR MINI 230V 50HZ 6481787 manufactured by Maquet Critical Care Ab.

MAUDE Entry Details

Report Number8010042-2019-00790
MDR Report Key9245657
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-10-28
Date of Report2019-10-28
Date of Event2019-09-22
Date Mfgr Received2019-10-21
Date Added to Maude2019-10-28
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 CRITICAL CARE AB R
Manufacturer CitySOLNA
Manufacturer CountrySW
Manufacturer G1MAGNUS LINDQVIST
Manufacturer StreetMAQUET CRITICAL CARE AB R
Manufacturer CitySOLNA
Manufacturer CountrySW
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCOMPRESSOR MINI
Generic NameCOMPRESSOR, AIR, PORTABLE
Product CodeBTI
Date Received2019-10-28
Model NumberCOMPR MINI 230V 50HZ
Catalog Number6481787
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerMAQUET CRITICAL CARE AB
Manufacturer AddressROENTGENVAGEN 2 SOLNA US


Patients

Patient NumberTreatmentOutcomeDate
10 2019-10-28

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