MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2019-06-19 for CATHETER PASSER, DISPOSABLE, 60 CM 48409 manufactured by Medtronic Neurosurgery.
Report Number | 2021898-2019-00239 |
MDR Report Key | 8713997 |
Report Source | FOREIGN,HEALTH PROFESSIONAL |
Date Received | 2019-06-19 |
Date of Report | 2019-09-13 |
Date of Event | 2019-06-12 |
Date Mfgr Received | 2019-08-23 |
Device Manufacturer Date | 2018-11-19 |
Date Added to Maude | 2019-06-19 |
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 MN 92618 |
Manufacturer Country | US |
Manufacturer Postal | 92618 |
Manufacturer Phone | 7635263305 |
Manufacturer G1 | MEDTRONIC NEUROSURGERY |
Manufacturer Street | 125 CREMONA DRIVE |
Manufacturer City | GOLETA CA 93117 |
Manufacturer Country | US |
Manufacturer Postal Code | 93117 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CATHETER PASSER, DISPOSABLE, 60 CM |
Generic Name | CATHETER, PERCUTANEOUS, INTRASPINAL, SHORT TERM |
Product Code | MAJ |
Date Received | 2019-06-19 |
Returned To Mfg | 2019-07-08 |
Model Number | 48409 |
Catalog Number | 48409 |
Lot Number | E57439 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MEDTRONIC NEUROSURGERY |
Manufacturer Address | 125 CREMONA DRIVE GOLETA CA 93117 US 93117 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-06-19 |