MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-03-10 for AMPLATZER DUCT OCCLUDER 9-PDA-006 manufactured by St. Jude Medical (cvd-minnetonka).
Report Number | 2182269-2020-00025 |
MDR Report Key | 9813332 |
Report Source | HEALTH PROFESSIONAL |
Date Received | 2020-03-10 |
Date of Report | 2020-03-10 |
Date of Event | 2020-02-14 |
Date Mfgr Received | 2020-02-28 |
Device Manufacturer Date | 2019-09-12 |
Date Added to Maude | 2020-03-10 |
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 | PAMELA YIP |
Manufacturer Street | 5050 NATHAN LANE N |
Manufacturer City | PLYMOUTH MN 55442 |
Manufacturer Country | US |
Manufacturer Postal | 55442 |
Manufacturer Phone | 6517565400 |
Manufacturer G1 | ST. JUDE MEDICAL (CVD-MINNETONKA) |
Manufacturer Street | 14901 DEVEAU PLACE |
Manufacturer City | MINNETONKA MN 553452126 |
Manufacturer Country | US |
Manufacturer Postal Code | 553452126 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | AMPLATZER DUCT OCCLUDER |
Generic Name | TRANSCATHETER SEPTAL OCCLUDER |
Product Code | MLV |
Date Received | 2020-03-10 |
Returned To Mfg | 2020-02-28 |
Model Number | 9-PDA-006 |
Catalog Number | 9-PDA-006 |
Lot Number | 7176841 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ST. JUDE MEDICAL (CVD-MINNETONKA) |
Manufacturer Address | 14901 DEVEAU PLACE MINNETONKA MN 553452126 US 553452126 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Hospitalization | 2020-03-10 |