MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-08-23 for ANGIOSCULPT PTA SCORING BALLOON CATHETER (OTW) 2076-5040 manufactured by Spectranetics.
Report Number | 3005462046-2019-00011 |
MDR Report Key | 8927441 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2019-08-23 |
Date of Report | 2019-08-10 |
Date of Event | 2019-08-07 |
Report Date | 2005-01-01 |
Date Reported to FDA | 2005-01-01 |
Date Reported to Mfgr | 2005-01-10 |
Date Mfgr Received | 2019-08-10 |
Device Manufacturer Date | 2019-02-18 |
Date Added to Maude | 2019-08-23 |
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 | MS. ANA TAN |
Manufacturer Street | 5055 BRANDIN COURT |
Manufacturer City | FREMONT CA 94538 |
Manufacturer Country | US |
Manufacturer Postal | 94538 |
Manufacturer Phone | 510933-798 |
Manufacturer G1 | SPECTRANETICS |
Manufacturer Street | 5055 BRANDIN COURT |
Manufacturer City | FREMONT CA 94538 |
Manufacturer Country | US |
Manufacturer Postal Code | 94538 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ANGIOSCULPT PTA SCORING BALLOON CATHETER (OTW) |
Generic Name | CATHETER, PERCUTANEOUS, CUTTING/SCORING |
Product Code | PNO |
Date Received | 2019-08-23 |
Model Number | 2076-5040 |
Catalog Number | 2076-5040 |
Lot Number | G19020017 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SPECTRANETICS |
Manufacturer Address | 5055 BRANDIN COURT FREMONT CA 94538 US 94538 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2019-08-23 |