MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,other report with the FDA on 2020-03-26 for CARPENTIER-EDWARDS? PERIMOUNT THEON? PERICARDIAL BIOPROSTHESIS 6900PTFX manufactured by Edwards Lifesciences.
Report Number | 2015691-2020-11163 |
MDR Report Key | 9886468 |
Report Source | HEALTH PROFESSIONAL,OTHER |
Date Received | 2020-03-26 |
Date of Report | 2020-03-04 |
Date of Event | 2020-02-26 |
Date Mfgr Received | 2020-03-04 |
Device Manufacturer Date | 2015-04-16 |
Date Added to Maude | 2020-03-26 |
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 | 1 EDWARDS WAY |
Manufacturer City | IRVINE CA 92614 |
Manufacturer Country | US |
Manufacturer Postal | 92614 |
Manufacturer Phone | 9492504062 |
Manufacturer G1 | EDWARDS LIFESCIENCES |
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 | CARPENTIER-EDWARDS? PERIMOUNT THEON? PERICARDIAL BIOPROSTHESIS |
Generic Name | REPLACEMENT HEART VALVE |
Product Code | DYE |
Date Received | 2020-03-26 |
Returned To Mfg | 2020-03-17 |
Model Number | 6900PTFX |
Device Expiration Date | 2019-04-15 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | Y |
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. Hospitalization; 2. Required No Informationntervention | 2020-03-26 |