INVOS DS5100C-PB

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 2019-09-25 for INVOS DS5100C-PB manufactured by Jabil Circuit(shanghai) Ltd.

MAUDE Entry Details

Report Number2936999-2019-00786
MDR Report Key9121206
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2019-09-25
Date of Report2019-11-15
Date Mfgr Received2019-10-29
Date Added to Maude2019-09-25
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 ContactAVI KLUGER
Manufacturer Street5920 LONGBOW DRIVE
Manufacturer CityBOULDER CO 80301
Manufacturer CountryUS
Manufacturer Postal80301
Manufacturer Phone3035306582
Manufacturer G1JABIL CIRCUIT(SHANGHAI) LTD
Manufacturer StreetNO 600 TIAN LIN RD
Manufacturer CitySHANGHAI 20023
Manufacturer CountryCN
Manufacturer Postal Code20023
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameINVOS
Generic NameOXIMETER, TISSUE SATURATION
Product CodeMUD
Date Received2019-09-25
Returned To Mfg2019-09-10
Model NumberDS5100C-PB
Catalog NumberDS5100C-PB
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerJABIL CIRCUIT(SHANGHAI) LTD
Manufacturer AddressNO 600 TIAN LIN RD SHANGHAI 20023 CN 20023


Patients

Patient NumberTreatmentOutcomeDate
10 2019-09-25

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