FLOWMETER MP01192

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-08-24 for FLOWMETER MP01192 manufactured by Dr?gerwerk Ag & Co. Kgaa.

Event Text Entries

[118393116] The investigation has just started; results will be provided in a follow-up report.
Patient Sequence No: 1, Text Type: N, H10


[118393117] It was reported that the pressure dome of a flowmeter came off from the main body when the device was put into operation (pressurized). There was no injury of a person reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9611500-2018-00267
MDR Report Key7812120
Date Received2018-08-24
Date of Report2018-09-28
Date of Event2018-07-16
Date Mfgr Received2018-09-25
Date Added to Maude2018-08-24
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 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 Report0

Device Details

Brand NameFLOWMETER
Generic NameFLOWMETER GAS
Product CodeCAX
Date Received2018-08-24
Model NumberNA
Catalog NumberMP01192
Lot NumberNA
Device Expiration Date2000-01-01
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
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 2018-08-24

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