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 2020-03-13 for MARATHON 105-5056 manufactured by Micro Therapeutics, Inc. Dba Ev3.
Report Number | 2029214-2020-00219 |
MDR Report Key | 9831989 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2020-03-13 |
Date of Report | 2020-03-13 |
Date of Event | 2020-03-10 |
Date Mfgr Received | 2020-03-10 |
Device Manufacturer Date | 2018-07-22 |
Date Added to Maude | 2020-03-13 |
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 | KATCHA TAYLOR |
Manufacturer Street | 9775 TOLEDO WAY |
Manufacturer City | IRVINE CA 92618 |
Manufacturer Country | US |
Manufacturer Postal | 92618 |
Manufacturer Phone | 9496801345 |
Manufacturer G1 | MICRO THERAPEUTICS, INC. DBA EV3 |
Manufacturer Street | 9775 TOLEDO WAY |
Manufacturer City | IRVINE CA 92618 |
Manufacturer Country | US |
Manufacturer Postal Code | 92618 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | MARATHON |
Generic Name | CATHETER, CONTINUOUS FLUSH |
Product Code | KRA |
Date Received | 2020-03-13 |
Model Number | 105-5056 |
Catalog Number | 105-5056 |
Lot Number | A683251 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MICRO THERAPEUTICS, INC. DBA EV3 |
Manufacturer Address | 9775 TOLEDO WAY IRVINE CA 92618 US 92618 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2020-03-13 |