MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-09-06 for SITE-RITE 8 ULTRASOUND SYSTEM W/PINPOINT GT 9770501 manufactured by Bard Access Systems.
| Report Number | 3006260740-2019-02625 |
| MDR Report Key | 8971654 |
| Date Received | 2019-09-06 |
| Date of Report | 2019-11-08 |
| Date Mfgr Received | 2019-10-11 |
| Date Added to Maude | 2019-09-06 |
| 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 | BIOMEDICAL ENGINEER |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | SYDNEY FRECKLETON |
| Manufacturer Street | 605 N. 5600 W. |
| Manufacturer City | SALT LAKE CITY UT 84116 |
| Manufacturer Country | US |
| Manufacturer Postal | 84116 |
| Manufacturer Phone | 8015225992 |
| Manufacturer G1 | DYMAX CORP. |
| Manufacturer Street | 141 ZEHNER SCHOOL ROAD |
| Manufacturer City | ZELIENOPLE PA 16063 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 16063 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Removal Correction Number | 2243072-10/11/2019-013-C |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | SITE-RITE 8 ULTRASOUND SYSTEM W/PINPOINT GT |
| Generic Name | SYSTEM, IMAGING, PULSED ECHO, ULTRASONIC |
| Product Code | ITX |
| Date Received | 2019-09-06 |
| Model Number | 9770501 |
| Catalog Number | 9770501 |
| Lot Number | N/A |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | DA |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | BARD ACCESS SYSTEMS |
| Manufacturer Address | 605 N. 5600 W. SALT LAKE CITY UT 84116 US 84116 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2019-09-06 |