MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,user facility report with the FDA on 2019-09-13 for SMITHS MEDICAL CENTRAL VENOUS CATHETERSDELTEC LOGICATH CONVENTIONAL MXA231X20X16V manufactured by Smiths Medical Asd, Inc..
Report Number | 3012307300-2019-04972 |
MDR Report Key | 9037828 |
Report Source | FOREIGN,USER FACILITY |
Date Received | 2019-09-13 |
Date of Report | 2019-10-08 |
Date of Event | 2019-05-01 |
Date Mfgr Received | 2019-09-19 |
Device Manufacturer Date | 2016-12-21 |
Date Added to Maude | 2019-09-13 |
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 | DAVE HALVERSON |
Manufacturer Street | 6000 NATHAN LANE NORTH |
Manufacturer City | MINNEAPOLIS MN 55442 |
Manufacturer Country | US |
Manufacturer Postal | 55442 |
Manufacturer Phone | 7633833310 |
Manufacturer G1 | SMITHS MEDICAL CZECH REPUBLIC A.S. |
Manufacturer Street | OLOMOUCK? 306 |
Manufacturer City | HRANICE, 753 01 |
Manufacturer Country | EZ |
Manufacturer Postal Code | 753 01 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | SMITHS MEDICAL CENTRAL VENOUS CATHETERSDELTEC LOGICATH CONVENTIONAL |
Generic Name | CENTRAL VENOUS CATHETER DRESSING CHANGE KIT |
Product Code | PEZ |
Date Received | 2019-09-13 |
Catalog Number | MXA231X20X16V |
Lot Number | 3337605C |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SMITHS MEDICAL ASD, INC. |
Manufacturer Address | 6000 NATHAN LANE NORTH MINNEAPOLIS MN 55442 US 55442 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-09-13 |