MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2019-11-26 for 18 FR. RMI ARTERIAL PERFUSION CANNULA II, 20 FR. RMI ARTERIAL PERFUSION CANNULA OPTI22 manufactured by Edwards Lifesciences.
Report Number | 3008500478-2019-00172 |
MDR Report Key | 9377193 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2019-11-26 |
Date of Report | 2019-11-07 |
Date of Event | 2019-11-07 |
Date Mfgr Received | 2019-11-07 |
Device Manufacturer Date | 2018-04-26 |
Date Added to Maude | 2019-11-26 |
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 | MS. AMRITHA SRINIVASAN |
Manufacturer Street | 12050 LONE PEAK PARKWAY MLE-2 |
Manufacturer City | DRAPER UT 84020 |
Manufacturer Country | US |
Manufacturer Postal | 84020 |
Manufacturer Phone | 9492504062 |
Manufacturer G1 | EDWARDS LIFESCIENCES LLC |
Manufacturer Street | 1 EDWARDS WAY |
Manufacturer City | IRVINE CA 92614 |
Manufacturer Country | US |
Manufacturer Postal Code | 92614 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | 18 FR. RMI ARTERIAL PERFUSION CANNULA II, 20 FR. RMI ARTERIAL PERFUSION CANNULA |
Generic Name | CANNULA, CATHETER |
Product Code | DQR |
Date Received | 2019-11-26 |
Model Number | OPTI22 |
Catalog Number | OPTI22 |
Lot Number | 61338640 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | EDWARDS LIFESCIENCES |
Manufacturer Address | 1 EDWARDS WAY IRVINE CA 92614 US 92614 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Life Threatening | 2019-11-26 |