MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-01-09 for AORTIC ARCH CANNULAE, OPTIFLOW AORTIC ARCH CANNULA A282-70A manufactured by Sorin Group Italia Srl.
Report Number | 9680841-2020-00003 |
MDR Report Key | 9568216 |
Report Source | HEALTH PROFESSIONAL |
Date Received | 2020-01-09 |
Date of Report | 2019-12-10 |
Date Mfgr Received | 2020-03-27 |
Device Manufacturer Date | 2019-11-11 |
Date Added to Maude | 2020-01-09 |
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 | ENRICO GRECO |
Manufacturer Street | 14401 W 65TH WAY |
Manufacturer City | ARVADA CO 80004 |
Manufacturer Country | US |
Manufacturer Postal | 80004 |
Manufacturer G1 | SORIN GROUP ITALIA SRL |
Manufacturer Street | STRADA STATALE 12 NORD, 86 |
Manufacturer City | MIRANDOLA 41037 |
Manufacturer Country | IT |
Manufacturer Postal Code | 41037 |
Single Use | 3 |
Remedial Action | OT |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | AORTIC ARCH CANNULAE, OPTIFLOW AORTIC ARCH CANNULA |
Generic Name | CATETHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS |
Product Code | DWF |
Date Received | 2020-01-09 |
Returned To Mfg | 2020-01-16 |
Model Number | A282-70A |
Catalog Number | A282-70A |
Lot Number | 1911110040 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SORIN GROUP ITALIA SRL |
Manufacturer Address | STRADA STATALE 12 NORD, 86 MIRANDOLA, MODENA US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-01-09 |