INVOS SAFB-SM/INTL

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-08-13 for INVOS SAFB-SM/INTL manufactured by Jabil Circuit(shanghai) Ltd.

MAUDE Entry Details

Report Number2936999-2019-00532
MDR Report Key8890626
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-08-13
Date of Report2019-08-13
Date of Event2019-07-24
Date Mfgr Received2019-07-24
Date Added to Maude2019-08-13
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 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 200233
Manufacturer CountryCN
Manufacturer Postal Code200233
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameINVOS
Generic NameOXIMETER, TISSUE SATURATION
Product CodeMUD
Date Received2019-08-13
Model NumberSAFB-SM/INTL
Catalog NumberSAFB-SM/INTL
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerJABIL CIRCUIT(SHANGHAI) LTD
Manufacturer AddressNO 600 TIAN LIN RD SHANGHAI 200233 CN 200233


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-08-13

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