LUCEA LED 40 MOBILE LUCEA40

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-08-05 for LUCEA LED 40 MOBILE LUCEA40 manufactured by Maquet S.a.s..

MAUDE Entry Details

Report Number8859439
MDR Report Key8859439
Date Received2019-08-05
Date of Report2019-07-25
Date of Event2019-06-21
Report Date2019-07-25
Date Reported to FDA2019-07-25
Date Reported to Mfgr2019-08-05
Date Added to Maude2019-08-05
Event Key0
Report Source CodeUser Facility report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag0
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameLUCEA LED 40 MOBILE
Generic NameLIGHT, SURGICAL, FLOOR STANDING
Product CodeFSS
Date Received2019-08-05
Model NumberLUCEA40
Device AvailabilityY
Device Age2 YR
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerMAQUET S.A.S.
Manufacturer Address45 BARBOUR POND DRIVE WAYNE NJ 07470 US 07470


Patients

Patient NumberTreatmentOutcomeDate
10 2019-08-05

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