FLOWMETER MP04560

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,user f report with the FDA on 2019-06-07 for FLOWMETER MP04560 manufactured by Dr?gerwerk Ag & Co. Kgaa.

MAUDE Entry Details

Report Number9611500-2019-00168
MDR Report Key8677498
Report SourceCOMPANY REPRESENTATIVE,USER F
Date Received2019-06-07
Date of Report2019-08-13
Date of Event2019-05-23
Date Mfgr Received2019-07-31
Date Added to Maude2019-06-07
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationBIOMEDICAL ENGINEER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. SONJA HILLMER
Manufacturer StreetMOISLINGER ALLEE 53-55
Manufacturer CityL 23542
Manufacturer CountryGM
Manufacturer Postal23542
Manufacturer Phone4518822868
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameFLOWMETER
Generic NameFLOWMETER, GAS
Product CodeBXY
Date Received2019-06-07
Model NumberNA
Catalog NumberMP04560
Lot NumberNA
Device Expiration Date2000-01-01
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerDR?GERWERK AG & CO. KGAA
Manufacturer AddressMOISLINGER ALLEE 53-55 L?BECK 23542 GM 23542


Patients

Patient NumberTreatmentOutcomeDate
10 2019-06-07

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