IMGMGMNT_PHOTOVIDEO SYSTEM 242325

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2019-10-25 for IMGMGMNT_PHOTOVIDEO SYSTEM 242325 manufactured by Depuy Mitek Llc Us.

MAUDE Entry Details

Report Number1221934-2019-59210
MDR Report Key9238904
Report SourceCOMPANY REPRESENTATIVE
Date Received2019-10-25
Date of Report2019-08-22
Date of Event2019-08-21
Date Mfgr Received2019-11-15
Date Added to Maude2019-10-25
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 ContactKARA DITTY-BOVARD
Manufacturer Street325 PARAMOUNT DRIVE
Manufacturer CityRAYNHAM MA 02767
Manufacturer CountryUS
Manufacturer Postal02767
Manufacturer Phone6103142063
Manufacturer G1JJMSZ PLANT FOR STK. & N-STK.
Manufacturer StreetNO. 299, CHANGYANG STREET SUZHOU INDUSTRIAL PARK
Manufacturer CitySUZHOU, JIANGSU 215126
Manufacturer CountryCH
Manufacturer Postal Code215126
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameIMGMGMNT_PHOTOVIDEO SYSTEM
Generic NameENDOSCOPE CAMERA ADAPTOR
Product CodeFEM
Date Received2019-10-25
Returned To Mfg2019-11-04
Catalog Number242325
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerDEPUY MITEK LLC US
Manufacturer Address325 PARAMOUNT DRIVE RAYNHAM MA 02767 US 02767


Patients

Patient NumberTreatmentOutcomeDate
10 2019-10-25

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.