ROUND KNIFE 45?, ? 2 MM, 16 CM 226820

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-01-27 for ROUND KNIFE 45?, ? 2 MM, 16 CM 226820 manufactured by Karl Storz Se & Co. Kg.

MAUDE Entry Details

Report Number9610617-2020-00010
MDR Report Key9634510
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-01-27
Date of Report2020-01-24
Date of Event2020-01-17
Date Mfgr Received2020-01-17
Device Manufacturer Date2005-05-15
Date Added to Maude2020-01-27
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 ContactMRS. SUSIE CHEN
Manufacturer Street2151 E. GRAND AVENUE
Manufacturer CityEL SEGUNDO CA 902455017
Manufacturer CountryUS
Manufacturer Postal902455017
Manufacturer Phone4242188201
Manufacturer G1KARL STORZ SE & CO. KG
Manufacturer StreetDR.-KARL-STORZ-STRASSE 34 78532
Manufacturer CityTUTTLINGEN,
Manufacturer CountryGM
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameROUND KNIFE 45?, ? 2 MM, 16 CM
Generic NameROUND KNIFE
Product CodeLRC
Date Received2020-01-27
Model Number226820
Catalog Number226820
Lot NumberTS01
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerKARL STORZ SE & CO. KG
Manufacturer AddressDR.-KARL-STORZ-STRASSE 34 78532 TUTTLINGEN, GM


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-01-27

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