MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-08-15 for SWAN-GANZ BIPOLAR PACING CATHETER FOR FEMORAL INSERTION PE075F5 manufactured by Edwards Lifesciences, Pr.
Report Number | 2015691-2019-03047 |
MDR Report Key | 8899133 |
Date Received | 2019-08-15 |
Date of Report | 2019-07-26 |
Date of Event | 2019-07-23 |
Date Mfgr Received | 2019-08-16 |
Device Manufacturer Date | 2017-10-04 |
Date Added to Maude | 2019-08-15 |
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 | MS. 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 PR 00610 |
Manufacturer Country | US |
Manufacturer Postal Code | 00610 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | SWAN-GANZ BIPOLAR PACING CATHETER FOR FEMORAL INSERTION |
Generic Name | PACING CATHETER |
Product Code | LDF |
Date Received | 2019-08-15 |
Model Number | PE075F5 |
Lot Number | 61038461 |
Device Expiration Date | 2019-09-16 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
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 PR 00610 US 00610 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-08-15 |