PELORIS RAPID TISSUE PROCESSOR PELORIS LL 26.0008

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 2020-03-20 for PELORIS RAPID TISSUE PROCESSOR PELORIS LL 26.0008 manufactured by Leica Biosystems Melbourne Pty. Ltd.

MAUDE Entry Details

Report Number8020030-2020-00011
MDR Report Key9859878
Report SourceCOMPANY REPRESENTATIVE
Date Received2020-03-20
Date of Report2020-03-20
Date of Event2020-02-21
Date Mfgr Received2020-02-25
Device Manufacturer Date2015-12-03
Date Added to Maude2020-03-20
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 ContactMRS ADRIENNE HARDISTY
Manufacturer Street495 BLACKBURN ROAD
Manufacturer CityMOUNT WAVERLEY, VIC 3149
Manufacturer CountryAS
Manufacturer Postal3149
Manufacturer G1LEICA BIOSYSTEMS MELBOURNE PTY. LTD
Manufacturer Street495 BLACKBURN ROAD
Manufacturer CityMOUNT WAVERLEY, VIC 3149
Manufacturer CountryAS
Manufacturer Postal Code3149
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePELORIS RAPID TISSUE PROCESSOR
Generic NameAUTOMATED TISSUE PROCESSOR
Product CodeIEO
Date Received2020-03-20
Model NumberPELORIS LL
Catalog Number26.0008
Device AvailabilityY
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerLEICA BIOSYSTEMS MELBOURNE PTY. LTD
Manufacturer Address495 BLACKBURN ROAD MOUNT WAVERLEY, VIC 3149 AS 3149


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-20

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