MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2020-01-17 for WEBSTER? ELECTROPHYSIOLOGY CATHETER 1086259RT manufactured by Biosense Webster Inc.
Report Number | 2029046-2020-00106 |
MDR Report Key | 9603669 |
Report Source | COMPANY REPRESENTATIVE |
Date Received | 2020-01-17 |
Date of Report | 2019-12-19 |
Date of Event | 2019-12-19 |
Date Mfgr Received | 2020-01-20 |
Device Manufacturer Date | 2019-10-31 |
Date Added to Maude | 2020-01-17 |
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. GABRIEL ALFAGEME |
Manufacturer Street | 31 TECHNOLOGY DRIVE |
Manufacturer City | IRVINE CA 92618 |
Manufacturer Country | US |
Manufacturer Postal | 92618 |
Manufacturer Phone | 949789-868 |
Manufacturer G1 | BIOSENSE WEBSTER INC (JUAREZ) |
Manufacturer Street | CIRCUITO INTERIOR NORTE 1820PARQUE INDUSTRIAL SALVACAR |
Manufacturer City | JUAREZ 32599 |
Manufacturer Country | MX |
Manufacturer Postal Code | 32599 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | WEBSTER? ELECTROPHYSIOLOGY CATHETER |
Generic Name | ELECTRODE, PACEMAKER, TEMPORARY |
Product Code | LDF |
Date Received | 2020-01-17 |
Model Number | 1086259RT |
Catalog Number | 1086259RT |
Lot Number | 30315387M |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BIOSENSE WEBSTER INC |
Manufacturer Address | 33 TECHNOLOGY DRIVE IRVINE CA 92618 US 92618 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Hospitalization; 2. Life Threatening; 3. Required No Informationntervention | 2020-01-17 |