MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,distri report with the FDA on 2019-06-21 for GUIDE WIRE ACC.KIT W/COPILOT 1003330 manufactured by Av-temecula-ct.
Report Number | 2024168-2019-04933 |
MDR Report Key | 8722232 |
Report Source | COMPANY REPRESENTATIVE,DISTRI |
Date Received | 2019-06-21 |
Date of Report | 2019-07-22 |
Date of Event | 2019-02-27 |
Date Mfgr Received | 2019-07-02 |
Device Manufacturer Date | 2018-03-01 |
Date Added to Maude | 2019-06-21 |
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 | CONNIE SPECK |
Manufacturer Street | ABBOTT VASCULAR 26531 YNEZ ROAD |
Manufacturer City | TEMECULA CA 925914628 |
Manufacturer Country | US |
Manufacturer Postal | 925914628 |
Manufacturer Phone | 9519143996 |
Manufacturer G1 | ABBOTT VASCULAR, TEMECULA, CA USA REG# 2024168 |
Manufacturer Street | ABBOTT VASCULAR 26531 YNEZ ROAD |
Manufacturer City | TEMECULA CA 925914628 |
Manufacturer Country | US |
Manufacturer Postal Code | 925914628 |
Single Use | 3 |
Remedial Action | OT |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | GUIDE WIRE ACC.KIT W/COPILOT |
Generic Name | HEMOSTATIC VALVE |
Product Code | DTL |
Date Received | 2019-06-21 |
Returned To Mfg | 2019-06-18 |
Catalog Number | 1003330 |
Lot Number | 60114359 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | AV-TEMECULA-CT |
Manufacturer Address | ABBOTT VASCULAR 26531 YNEZ ROAD TEMECULA CA 925914628 US 925914628 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-06-21 |