MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-03-23 for SYNCHRO2-14 SOFT STRAIGHT 200CM M00326010 manufactured by Stryker Neurovascular-utah-salt Lake City.
Report Number | 3012931345-2020-00045 |
MDR Report Key | 9868271 |
Report Source | HEALTH PROFESSIONAL |
Date Received | 2020-03-23 |
Date of Report | 2020-03-23 |
Date of Event | 2020-03-03 |
Date Mfgr Received | 2020-03-03 |
Date Added to Maude | 2020-03-23 |
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. TARA LOPEZ |
Manufacturer Street | 47900 BAYSIDE PARKWAY |
Manufacturer City | FREMONT CA 94538 |
Manufacturer Country | US |
Manufacturer Postal | 94538 |
Manufacturer Phone | 5104132500 |
Manufacturer G1 | STRYKER NEUROVASCULAR-UTAH-SALT LAKE CITY |
Manufacturer Street | 4870 WEST 2100 SOUTH |
Manufacturer City | SALT LAKE CITY UT 84120 |
Manufacturer Country | US |
Manufacturer Postal Code | 84120 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | SYNCHRO2-14 SOFT STRAIGHT 200CM |
Generic Name | WIRE, GUIDE, CATHETER |
Product Code | DQX |
Date Received | 2020-03-23 |
Returned To Mfg | 2020-03-13 |
Model Number | M00326010 |
Catalog Number | M00326010 |
Lot Number | 0000039309 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | STRYKER NEUROVASCULAR-UTAH-SALT LAKE CITY |
Manufacturer Address | 4870 WEST 2100 SOUTH SALT LAKE CITY UT 84120 US 84120 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-23 |