LOGOS 61502/140

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-02-21 for LOGOS 61502/140 manufactured by Milestone S.r.l..

MAUDE Entry Details

Report Number1000391282-2020-00001
MDR Report Key9738970
Date Received2020-02-21
Date of Report2020-02-21
Date Mfgr Received2020-01-29
Device Manufacturer Date2014-06-11
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 Professional0
Initial Report to FDA0
Report to FDA3
Event Location3
Manufacturer ContactMR. FRANCESCO VISINONI
Manufacturer StreetVIA FATEBENEFRATELLI, 1/5
Manufacturer CitySORISOLE, BERGAMO 24010
Manufacturer CountryIT
Manufacturer Postal24010
Manufacturer G1MILESTONE S.R.L.
Manufacturer StreetVIA FATEBENEFRATELLI, 1/5
Manufacturer CitySORISOLE, BERGAMO 24010
Manufacturer CountryIT
Manufacturer Postal Code24010
Single Use3
Remedial ActionOT
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameLOGOS
Generic NameAUTOMATED TISSUE PROCESSOR
Product CodeIEO
Date Received2020-02-21
Model Number61502/140
Catalog Number61502/140
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerMILESTONE S.R.L.
Manufacturer AddressVIA FATEBENEFRATELLI, 1/5 SORISOLE, BERGAMO 24010 IT 24010


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-02-21

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