HYALURONIC ACID 89122-0724-20

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a other report with the FDA on 2020-03-04 for HYALURONIC ACID 89122-0724-20 manufactured by Fidia Farmaceutici S.p.a..

MAUDE Entry Details

Report Number9610200-2020-00001
MDR Report Key9784628
Report SourceOTHER
Date Received2020-03-04
Date of Report2020-03-04
Date of Event2020-01-21
Date Mfgr Received2020-02-07
Date Added to Maude2020-03-04
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. GIUSEPPE DI SANTE
Manufacturer StreetVIA PONTE DELLA FABBRICA, 3/A
Manufacturer CityABANO TERME, PADUA 35031
Manufacturer CountryIT
Manufacturer Postal35031
Manufacturer G1FIDIA FARMACEUTICI S.P.A.
Manufacturer StreetVIA PONTE DELLA FABBRICA, 3/A
Manufacturer CityABANO TERME, PADUA 35031
Manufacturer CountryIT
Manufacturer Postal Code35031
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameHYALURONIC ACID
Generic NameSODIUM HYALURONATE
Product CodeMOZ
Date Received2020-03-04
Catalog Number89122-0724-20
Lot NumberUNK
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerFIDIA FARMACEUTICI S.P.A.
Manufacturer AddressVIA PONTE DELLA FABBRICA, 3A ABANO TERME, PADUA 35031 IT 35031


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization 2020-03-04

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