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 2020-03-09 for FOGARTY ARTERIAL EMBOLECTOMY CATHETER 120602F manufactured by Edwards Lifesciences Pr.
Report Number | 2015691-2020-10864 |
MDR Report Key | 9806288 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2020-03-09 |
Date of Report | 2020-01-20 |
Date of Event | 2020-01-20 |
Date Mfgr Received | 2020-02-16 |
Device Manufacturer Date | 2019-04-04 |
Date Added to Maude | 2020-03-09 |
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 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MRS SAMANTHA EVELEIGH |
Manufacturer Street | 1 EDWARDS WAY |
Manufacturer City | IRVINE CA 92614 |
Manufacturer Country | US |
Manufacturer Postal | 92614 |
Manufacturer Phone | 9492503939 |
Manufacturer G1 | EDWARDS LIFESCIENCES PR |
Manufacturer Street | STATE RD INDUS PK 402 KM 1.4 |
Manufacturer City | ANASCO 00610 |
Manufacturer Country | * |
Manufacturer Postal Code | 00610 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | FOGARTY ARTERIAL EMBOLECTOMY CATHETER |
Generic Name | CATHETER, EMBOLECTOMY |
Product Code | DXE |
Date Received | 2020-03-09 |
Returned To Mfg | 2020-02-02 |
Model Number | 120602F |
Catalog Number | 120602F |
Lot Number | 62086602 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | EDWARDS LIFESCIENCES PR |
Manufacturer Address | STATE RD INDUS PK 402 KM 1.4 ANASCO * |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-09 |