MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-02-26 for OMNICELL I.V.STATION ONCO I.V. STATION ONCO manufactured by Aesynt Incorporated.
| Report Number | 3011278888-2020-00004 |
| MDR Report Key | 9758459 |
| Report Source | HEALTH PROFESSIONAL |
| Date Received | 2020-02-26 |
| Date of Report | 2020-02-26 |
| Date of Event | 2020-02-04 |
| Date Mfgr Received | 2020-02-04 |
| Device Manufacturer Date | 2016-01-01 |
| Date Added to Maude | 2020-02-26 |
| 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 | MR. DAVID VANELLA |
| Manufacturer Street | 500 CRANBERRY WOODS DRIVE SUITE 400 |
| Manufacturer City | CRANBERRY TOWNSHIP, PA |
| Manufacturer Country | US |
| Manufacturer Phone | 7418115 |
| Manufacturer G1 | HEALTH ROBOTICS |
| Manufacturer Street | KRASKA ULICA, 4 |
| Manufacturer City | SEZANA, 6210 |
| Manufacturer Country | SI |
| Manufacturer Postal Code | 6210 |
| Single Use | 3 |
| Remedial Action | OT |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | OMNICELL I.V.STATION ONCO |
| Generic Name | PHARMACY COMPOUNDING DEVICE |
| Product Code | NEP |
| Date Received | 2020-02-26 |
| Model Number | I.V. STATION ONCO |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | AESYNT INCORPORATED |
| Manufacturer Address | 51 PENNWOOD PLACE WARRENDALE, PA US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2020-02-26 |