MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-09-26 for AUTOMATED IMPELLA CONTROLLER IMPELLA AIC CONTROLLER 0042-0000-EU manufactured by Abiomed Inc..
Report Number | 1220648-2019-00201 |
MDR Report Key | 9124428 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2019-09-26 |
Date of Report | 2019-09-26 |
Date of Event | 2019-09-17 |
Date Facility Aware | 2019-09-17 |
Date Mfgr Received | 2019-09-17 |
Device Manufacturer Date | 2018-12-13 |
Date Added to Maude | 2019-09-26 |
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 | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MR. RALPH BARISANO |
Manufacturer Street | 22 CHERRY HILL DRIVE |
Manufacturer City | DANVERS MA 01923 |
Manufacturer Country | US |
Manufacturer Postal | 01923 |
Manufacturer Phone | 9786461400 |
Manufacturer G1 | ABIOMED INC. |
Manufacturer Street | 22 CHERRY HILL DRIVE |
Manufacturer City | DANVERS MA 01923 |
Manufacturer Country | US |
Manufacturer Postal Code | 01923 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | AUTOMATED IMPELLA CONTROLLER |
Generic Name | AUTOMATED IMPELLA CONTROLLER |
Product Code | PYX |
Date Received | 2019-09-26 |
Model Number | IMPELLA AIC CONTROLLER |
Catalog Number | 0042-0000-EU |
Lot Number | 1380525 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ABIOMED INC. |
Manufacturer Address | 22 CHERRY HILL DRIVE DANVERS MA 01923 US 01923 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Hospitalization; 2. Required No Informationntervention | 2019-09-26 |