PIRANHA SUCTION PUMP 2208.001

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,u report with the FDA on 2019-11-15 for PIRANHA SUCTION PUMP 2208.001 manufactured by Richard Wolf Gmbh.

MAUDE Entry Details

Report Number9611102-2019-00033
MDR Report Key9331225
Report SourceFOREIGN,HEALTH PROFESSIONAL,U
Date Received2019-11-15
Date of Report2019-10-15
Date of Event2019-10-09
Date Mfgr Received2019-10-15
Device Manufacturer Date2016-02-03
Date Added to Maude2019-11-15
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 ContactMR. OLIVER EHRLICH
Manufacturer StreetPFORZHEIMER STREET 32
Manufacturer CityKNITTLINGEN, 75438
Manufacturer CountryGM
Manufacturer Postal75438
Manufacturer G1RICHARD WOLF GMBH
Manufacturer StreetPFORZHEIMER STREET 32
Manufacturer CityKNITTLINGEN, 75438
Manufacturer CountryGM
Manufacturer Postal Code75438
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePIRANHA SUCTION PUMP
Generic NamePOWERED SUCTION PUMP
Product CodeJCX
Date Received2019-11-15
Model Number2208.001
Catalog Number2208.001
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerRICHARD WOLF GMBH
Manufacturer AddressPFORZHEIMER STREET 32 KNITTLINGEN, 75438 GM 75438


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization 2019-11-15

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