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 2019-08-28 for LOGOS 61502/140 manufactured by Milestone S.r.l..

MAUDE Entry Details

Report Number1000391282-2019-00001
MDR Report Key8938652
Date Received2019-08-28
Date of Report2019-08-28
Date of Event2019-08-01
Date Mfgr Received2019-08-07
Device Manufacturer Date2015-03-20
Date Added to Maude2019-08-28
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 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, 24010
Manufacturer CountryIT
Manufacturer Postal Code24010
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameLOGOS
Generic NameAUTOMATED TISSUE PROCESSOR
Product CodeIEO
Date Received2019-08-28
Model Number61502/140
Catalog Number61502/140
Device Expiration Date2015-03-20
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Age4 YR
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerMILESTONE S.R.L.
Manufacturer AddressVIA FATEBENEFRATELLI, 1/5 SORISOLE, 24010 IT 24010


Patients

Patient NumberTreatmentOutcomeDate
10 2019-08-28

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