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 2020-03-16 for ACHIEVE ADVANCE MAPPING CATHETER 2ACH20 manufactured by Medtronic Mexico.
[183563569]
If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10
[183563570]
It was reported that post-operative to a successful cryo ablation procedure, the patient experienced "pericardial pain". The patient was treated with medication. The patient is a participant in a clinical study. No further patient complications have been reported as a result of this event.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 9612164-2020-01197 |
MDR Report Key | 9836596 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2020-03-16 |
Date of Report | 2020-03-16 |
Date of Event | 2018-10-12 |
Date Mfgr Received | 2020-02-21 |
Date Added to Maude | 2020-03-16 |
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 MEXICO |
Manufacturer Street | AV. PASEO DEL CUCAPAH #10510 |
Manufacturer City | TIJUANA,BC 22570 |
Manufacturer Country | MX |
Manufacturer Postal Code | 22570 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ACHIEVE ADVANCE MAPPING CATHETER |
Generic Name | CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING |
Product Code | DRF |
Date Received | 2020-03-16 |
Model Number | 2ACH20 |
Catalog Number | 2ACH20 |
Lot Number | 11034510 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MEDTRONIC MEXICO |
Manufacturer Address | AV. PASEO DEL CUCAPAH #10510 TIJUANA,BC 22570 MX 22570 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 2 | 1. Required No Informationntervention | 2020-03-16 |