MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2020-03-25 for SITE-RITE 8 ULTRASOUND SYSTSEM CONSOLE (REMANUFACTURED) 9770600Y manufactured by Bard Access Systems.
Report Number | 3006260740-2020-00992 |
MDR Report Key | 9877849 |
Report Source | COMPANY REPRESENTATIVE |
Date Received | 2020-03-25 |
Date of Report | 2020-03-25 |
Date Mfgr Received | 2020-03-02 |
Date Added to Maude | 2020-03-25 |
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 | SHELLY GILBERT |
Manufacturer Street | 605 N. 5600 W. |
Manufacturer City | SALT LAKE CITY UT 84116 |
Manufacturer Country | US |
Manufacturer Postal | 84116 |
Manufacturer Phone | 8015225640 |
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 |
Remedial Action | NO |
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 SYSTSEM CONSOLE (REMANUFACTURED) |
Generic Name | SYSTEM, IMAGING, PULSED ECHO, ULTRASONIC |
Product Code | IYO |
Date Received | 2020-03-25 |
Model Number | 9770600Y |
Catalog Number | 9770600Y |
Lot Number | N/A |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
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 | 2020-03-25 |