MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2019-06-13 for SHOCKWAVE S4 PERIPHERAL IVL CATHETER 61163-3540 S4IVL3540 manufactured by Shockwave Medical, Inc..
Report Number | 3010940016-2019-00002 |
MDR Report Key | 8697738 |
Report Source | COMPANY REPRESENTATIVE |
Date Received | 2019-06-13 |
Date of Report | 2019-06-13 |
Date of Event | 2019-05-16 |
Date Mfgr Received | 2019-05-16 |
Device Manufacturer Date | 2019-01-08 |
Date Added to Maude | 2019-06-13 |
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 | 48501 WARM SPRINGS BLVD. SUITE 108 |
Manufacturer City | FREMONT CA 94539 |
Manufacturer Country | US |
Manufacturer Postal | 94539 |
Manufacturer Phone | 5106249076 |
Manufacturer G1 | SHOCKWAVE MEDICAL, INC |
Manufacturer Street | 48501 WARM SPRINGS BLVD. SUITE 108 |
Manufacturer City | FREMONT CA 94539 |
Manufacturer Country | US |
Manufacturer Postal Code | 94539 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | SHOCKWAVE S4 PERIPHERAL IVL CATHETER |
Generic Name | BALLOON CATHETER |
Product Code | PPN |
Date Received | 2019-06-13 |
Model Number | 61163-3540 |
Catalog Number | S4IVL3540 |
Lot Number | P190108C |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SHOCKWAVE MEDICAL, INC. |
Manufacturer Address | 48501 WARM SPRINGS BLVD. SUITE 108 FREMONT CA 94539 US 94539 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Hospitalization; 2. Required No Informationntervention | 2019-06-13 |