SINGLE USE RETRIEVAL NITINOL BASKET V FG-V451P

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2019-06-27 for SINGLE USE RETRIEVAL NITINOL BASKET V FG-V451P manufactured by Olympus Medical Systems Corp..

MAUDE Entry Details

Report Number8010047-2019-02357
MDR Report Key8742494
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2019-06-27
Date of Report2019-07-11
Date of Event2019-05-22
Date Mfgr Received2019-06-17
Device Manufacturer Date2018-08-21
Date Added to Maude2019-06-27
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 ContactMR KAZUTAKA MATSUMOTO
Manufacturer Street2951 ISHIKAWA-CHO
Manufacturer CityHACHIOJI-SHI, TOKYO-TO 192-8507
Manufacturer CountryJA
Manufacturer Postal192-8507
Manufacturer Phone426425177
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSINGLE USE RETRIEVAL NITINOL BASKET V
Generic NameSINGLE USE RETRIEVAL BASKET
Product CodeLQR
Date Received2019-06-27
Model NumberFG-V451P
Lot Number91K
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerOLYMPUS MEDICAL SYSTEMS CORP.
Manufacturer Address2951 ISHIKAWA-CHO HACHIOJI-SHI, TOKYO-TO 192-8507 JA 192-8507


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-06-27

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