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..
Report Number | 9610200-2020-00001 |
MDR Report Key | 9784628 |
Report Source | OTHER |
Date Received | 2020-03-04 |
Date of Report | 2020-03-04 |
Date of Event | 2020-01-21 |
Date Mfgr Received | 2020-02-07 |
Date Added to Maude | 2020-03-04 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Health Professional | 0 |
Initial Report to FDA | 0 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MR. GIUSEPPE DI SANTE |
Manufacturer Street | VIA PONTE DELLA FABBRICA, 3/A |
Manufacturer City | ABANO TERME, PADUA 35031 |
Manufacturer Country | IT |
Manufacturer Postal | 35031 |
Manufacturer G1 | FIDIA FARMACEUTICI S.P.A. |
Manufacturer Street | VIA PONTE DELLA FABBRICA, 3/A |
Manufacturer City | ABANO TERME, PADUA 35031 |
Manufacturer Country | IT |
Manufacturer Postal Code | 35031 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | HYALURONIC ACID |
Generic Name | SODIUM HYALURONATE |
Product Code | MOZ |
Date Received | 2020-03-04 |
Catalog Number | 89122-0724-20 |
Lot Number | UNK |
Device Availability | N |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | FIDIA FARMACEUTICI S.P.A. |
Manufacturer Address | VIA PONTE DELLA FABBRICA, 3A ABANO TERME, PADUA 35031 IT 35031 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Hospitalization | 2020-03-04 |