LAPARO-CO2-PNEU 2232 FR 2232.641

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2020-02-07 for LAPARO-CO2-PNEU 2232 FR 2232.641 manufactured by Richard Wolf Gmbh.

MAUDE Entry Details

Report Number1418479-2020-00002
MDR Report Key9682270
Report SourceUSER FACILITY
Date Received2020-02-07
Date of Report2020-01-08
Date Facility Aware2020-01-08
Report Date2020-02-07
Date Reported to FDA2020-02-07
Date Reported to Mfgr2020-02-07
Date Mfgr Received2020-02-07
Date Added to Maude2020-02-07
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 NameLAPARO-CO2-PNEU 2232 FR
Generic NameLAPAROSCOPIC INSUFFLATOR
Product CodeHIF
Date Received2020-02-07
Returned To Mfg2020-01-23
Model Number2232.641
Catalog Number2232.641
Device AvailabilityR
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. Other 2020-02-07

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