SIR-SPHERES? Y-90 RESIN MICROSPHERES

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,s report with the FDA on 2020-02-21 for SIR-SPHERES? Y-90 RESIN MICROSPHERES manufactured by Sirtex Technology Pty Ltd.

MAUDE Entry Details

Report Number3005579300-2020-00003
MDR Report Key9738521
Report SourceFOREIGN,HEALTH PROFESSIONAL,S
Date Received2020-02-21
Date of Report2020-03-16
Date of Event2019-11-13
Date Mfgr Received2020-03-09
Date Added to Maude2020-02-21
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 StreetSHOP 6 207 PACIFIC HIGHWAY
Manufacturer CityST LEONARDS, 2065
Manufacturer CountryAS
Manufacturer Postal2065
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSIR-SPHERES? Y-90 RESIN MICROSPHERES
Generic NameMICEOSPHERES
Product CodeNAW
Date Received2020-02-21
Lot NumberNI403V09
OperatorHEALTH PROFESSIONAL
Device Availability*
Device AgeDA
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerSIRTEX TECHNOLOGY PTY LTD
Manufacturer AddressSHOP 6 207 PACIFIC HIGHWAY ST LEONARDS, 2065 AS 2065


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization 2020-02-21

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