MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-03-17 for LEAD EXTRACTION EVOLUTION RL CONTROLLED-ROTATION DILATOR SHEATH SET G23747 LR-EVN-13.0-RL manufactured by Cook Vandergrift Inc.
Report Number | 2522007-2020-00012 |
MDR Report Key | 9842062 |
Report Source | HEALTH PROFESSIONAL |
Date Received | 2020-03-17 |
Date of Report | 2020-03-16 |
Date of Event | 2020-02-17 |
Device Manufacturer Date | 2019-10-28 |
Date Added to Maude | 2020-03-17 |
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. BRIAN JOHNSTON |
Manufacturer Street | 1186 MONTGOMERY LANE |
Manufacturer City | VANDERGRIFT PA 15690 |
Manufacturer Country | US |
Manufacturer Postal | 15690 |
Manufacturer Phone | 7248458621 |
Manufacturer G1 | COOK VANDERGRIFT INC |
Manufacturer Street | 1186 MONTGOMERY LANE |
Manufacturer City | VANDERGRIFT PA 15690 |
Manufacturer Country | US |
Manufacturer Postal Code | 15690 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | LEAD EXTRACTION EVOLUTION RL CONTROLLED-ROTATION DILATOR SHEATH SET |
Generic Name | VESSEL DILATOR FOR PERCUTANEOUS CATHETERIZATION |
Product Code | DRE |
Date Received | 2020-03-17 |
Model Number | G23747 |
Catalog Number | LR-EVN-13.0-RL |
Lot Number | N167520 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | COOK VANDERGRIFT INC |
Manufacturer Address | 1186 MONTGOMERY LANE VANDERGRIFT PA 15690 US 15690 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2020-03-17 |