MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-10-11 for SARNS 8000 PERFUSION SYSTEM 195240 manufactured by Terumo Cardiovascular Systems Corporation.
        [90309589]
(b)(4). Per the customer, the sensors were mounted on an area that was curved.
 Patient Sequence No: 1, Text Type: N, H10
        [90309590]
It was reported that during set-up of the device for a cardiopulmonary bypass (cpb) procedure, the customer went through a box of level sensor pads before they could get one to stick. As a result, an alternate device was employed. The surgical procedure was completed successfully. There was no delay, no blood loss, nor adverse consequences to the patient.
 Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1828100-2017-00463 | 
| MDR Report Key | 6941061 | 
| Date Received | 2017-10-11 | 
| Date of Report | 2018-04-06 | 
| Date of Event | 2017-09-18 | 
| Date Mfgr Received | 2018-04-06 | 
| Date Added to Maude | 2017-10-11 | 
| 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. EILEEN DORSEY | 
| Manufacturer Street | 6200 JACKSON ROAD | 
| Manufacturer City | ANN ARBOR MI 48103 | 
| Manufacturer Country | US | 
| Manufacturer Postal | 48103 | 
| Manufacturer Phone | 7346634145 | 
| Single Use | 3 | 
| Previous Use Code | 3 | 
| Event Type | 3 | 
| Type of Report | 0 | 
| Brand Name | SARNS 8000 PERFUSION SYSTEM | 
| Generic Name | MONITOR AND/OR CONTROL, LEVEL SENSING, CARDIOPULMONARY BYPASS-SARNS 8000 | 
| Product Code | DTW | 
| Date Received | 2017-10-11 | 
| Model Number | 195240 | 
| Catalog Number | 195240 | 
| Operator | HEALTH PROFESSIONAL | 
| Device Availability | Y | 
| Device Age | DA | 
| Device Eval'ed by Mfgr | Y | 
| Device Sequence No | 1 | 
| Device Event Key | 0 | 
| Manufacturer | TERUMO CARDIOVASCULAR SYSTEMS CORPORATION | 
| Manufacturer Address | 6200 JACKSON ROAD ANN ARBOR MI 48103 US 48103 | 
| Patient Number | Treatment | Outcome | Date | 
|---|---|---|---|
| 1 | 0 | 2017-10-11 |