MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2019-10-17 for ZINGER XT LVZRXT180J manufactured by Medtronic, Inc.
Report Number | 1220452-2019-00136 |
MDR Report Key | 9205471 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2019-10-17 |
Date of Report | 2019-10-17 |
Date of Event | 2019-09-26 |
Date Mfgr Received | 2019-09-26 |
Device Manufacturer Date | 2018-10-25 |
Date Added to Maude | 2019-10-17 |
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 | PAULA BIXBY |
Manufacturer Street | 8200 CORAL SEA ST NE |
Manufacturer City | MOUNDS VIEW MN 55112 |
Manufacturer Country | US |
Manufacturer Postal | 55112 |
Manufacturer Phone | 7635055378 |
Manufacturer G1 | MEDTRONIC, INC |
Manufacturer Street | 37A CHERRY HILL DR |
Manufacturer City | DANVERS MA 01923 |
Manufacturer Country | US |
Manufacturer Postal Code | 01923 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ZINGER XT |
Generic Name | OCCLUDER, CATHETER TIP |
Product Code | DQT |
Date Received | 2019-10-17 |
Model Number | LVZRXT180J |
Catalog Number | LVZRXT180J |
Lot Number | G18A10971 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MEDTRONIC, INC |
Manufacturer Address | 37A CHERRY HILL DR DANVERS MA 01923 US 01923 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-10-17 |