MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-03-18 for CARBOMEDICS STANDARD PROSTHETIC HEART VALVE, AORTIC A5-021 manufactured by Sorin Group Italia Srl.
Report Number | 1718850-2020-01043 |
MDR Report Key | 9851301 |
Date Received | 2020-03-18 |
Date of Report | 2020-03-18 |
Date of Event | 2014-08-29 |
Date Facility Aware | 2020-02-18 |
Report Date | 2020-02-18 |
Date Reported to Mfgr | 2020-02-18 |
Date Mfgr Received | 2020-01-28 |
Date Added to Maude | 2020-03-18 |
Event Key | 0 |
Report Source Code | Distributor report |
Manufacturer Link | N |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Country | US |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CARBOMEDICS STANDARD PROSTHETIC HEART VALVE, AORTIC |
Generic Name | MECHANICAL HEART VALVE |
Product Code | LWQ |
Date Received | 2020-03-18 |
Model Number | A5-021 |
Catalog Number | A5-021 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SORIN GROUP ITALIA SRL |
Manufacturer Address | STRADA CRESCENTINO SNC SALUGGIA, VERCELLI 13040 IT 13040 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other; 2. Deathisabilit | 2020-03-18 |