MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-07-15 for AXS UNIVERSAL LINER SET (PACK OF 3) 077.0194 manufactured by Stryker Neurovascular Cork.
Report Number | 3008881809-2019-00205 |
MDR Report Key | 8789526 |
Date Received | 2019-07-15 |
Date of Report | 2019-09-13 |
Date of Event | 2019-06-19 |
Date Mfgr Received | 2019-09-04 |
Date Added to Maude | 2019-07-15 |
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 CORK |
Manufacturer Street | IDA INDUSTRIAL ESTATE MODEL FARM ROAD |
Manufacturer City | CORK NA |
Manufacturer Postal Code | NA |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | AXS UNIVERSAL LINER SET (PACK OF 3) |
Generic Name | PUMP, PORTABLE, ASPIRATION (MANUAL OR POWERED) |
Product Code | BTA |
Date Received | 2019-07-15 |
Catalog Number | 077.0194 |
Lot Number | 180514 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | STRYKER NEUROVASCULAR CORK |
Manufacturer Address | IDA INDUSTRIAL ESTATE MODEL FARM ROAD CORK NA NA |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-07-15 |