MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2020-03-06 for UNKNOWN STRATA VALVE/SHUNT UNKNOWN-S manufactured by Medtronic Neurosurgery.
Report Number | 2021898-2020-00088 |
MDR Report Key | 9800746 |
Report Source | CONSUMER |
Date Received | 2020-03-06 |
Date of Report | 2020-03-06 |
Date of Event | 2020-02-28 |
Date Mfgr Received | 2020-03-04 |
Date Added to Maude | 2020-03-06 |
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 | 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 | UNKNOWN STRATA VALVE/SHUNT |
Generic Name | SHUNT, CENTRAL NERVOUS SYSTEM AND COMPONENTS |
Product Code | JXG |
Date Received | 2020-03-06 |
Model Number | UNKNOWN-S |
Catalog Number | UNKNOWN-S |
Lot Number | UNKNOWN |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | * |
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 | 2020-03-06 |