MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2020-01-08 for PERIPHERAL INTRAVASCULAR LITHOTRIPSY (IVL) CATHETER FG62868-7060 manufactured by Shockwave Medical, Inc.
Report Number | 3015053858-2020-00001 |
MDR Report Key | 9565959 |
Report Source | COMPANY REPRESENTATIVE |
Date Received | 2020-01-08 |
Date of Report | 2019-12-13 |
Date of Event | 2019-12-13 |
Date Mfgr Received | 2019-12-13 |
Device Manufacturer Date | 2019-10-09 |
Date Added to Maude | 2020-01-08 |
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. RYAN KIRTLAND |
Manufacturer Street | 5403 BETSY ROSS DRIVE |
Manufacturer City | SANTA CLARA CA 95054 |
Manufacturer Country | US |
Manufacturer Postal | 95054 |
Manufacturer Phone | 4085502607 |
Manufacturer G1 | SHOCKWAVE MEDICAL, INC |
Manufacturer Street | 5403 BETSY ROSS DRIVE |
Manufacturer City | SANTA CLARA CA 95054 |
Manufacturer Country | US |
Manufacturer Postal Code | 95054 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | PERIPHERAL INTRAVASCULAR LITHOTRIPSY (IVL) CATHETER |
Generic Name | BALLOON CATHETER |
Product Code | PPN |
Date Received | 2020-01-08 |
Returned To Mfg | 2019-12-30 |
Model Number | FG62868-7060 |
Lot Number | P191009D |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SHOCKWAVE MEDICAL, INC |
Manufacturer Address | 5403 BETSY ROSS DRIVE SANTA CLARA CA 95054 US 95054 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2020-01-08 |