MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2019-12-06 for SMART, PERFUSION PACKS, CONNECTORS, TUBING 046001104 manufactured by Livanova Usa Inc.
Report Number | 1718850-2019-00024 |
MDR Report Key | 9422668 |
Report Source | HEALTH PROFESSIONAL |
Date Received | 2019-12-06 |
Date of Report | 2020-02-25 |
Date of Event | 2019-11-08 |
Date Mfgr Received | 2020-01-27 |
Device Manufacturer Date | 2019-08-01 |
Date Added to Maude | 2019-12-06 |
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 | ENRICO GRECO |
Manufacturer Street | 14401 W 65TH WAY |
Manufacturer City | ARVADA CO 80004 |
Manufacturer Country | US |
Manufacturer Postal | 80004 |
Manufacturer G1 | LIVANOVA USA INC |
Manufacturer Street | 14401 W 65TH WAY |
Manufacturer City | ARVADA CO 80004 |
Manufacturer Country | US |
Manufacturer Postal Code | 80004 |
Single Use | 3 |
Remedial Action | OT |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | SMART, PERFUSION PACKS, CONNECTORS, TUBING |
Generic Name | COBE SMARXT TUBING AND CONNECTORS |
Product Code | DWE |
Date Received | 2019-12-06 |
Catalog Number | 046001104 |
Lot Number | 1921300041 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | LIVANOVA USA INC |
Manufacturer Address | 14401 W 65TH WAY ARVADA CO 80004 US 80004 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-12-06 |