MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2019-04-11 for DIMENSION VISTA? K6454 SMN 10463378 manufactured by Siemens Healthcare Diagnostics Inc.
Report Number | 2517506-2019-00151 |
MDR Report Key | 8506099 |
Report Source | HEALTH PROFESSIONAL,USER FACI |
Date Received | 2019-04-11 |
Date of Report | 2019-04-11 |
Date of Event | 2019-03-13 |
Date Mfgr Received | 2019-03-18 |
Device Manufacturer Date | 2018-11-05 |
Date Added to Maude | 2019-04-11 |
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 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | JAMES MORGERA |
Manufacturer Street | 500 GBC DRIVE PO BOX 6101 |
Manufacturer City | NEWARK DE 197146101 |
Manufacturer Country | US |
Manufacturer Postal | 197146101 |
Manufacturer G1 | SIEMENS HEALTHCARE DIAGNOSTICS INC |
Manufacturer Street | 500 GBC DRIVE P.O. BOS 6101 |
Manufacturer City | NEWARK DE 197146101 |
Manufacturer Country | US |
Manufacturer Postal Code | 197146101 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | DIMENSION VISTA? |
Generic Name | DIMENSION VISTA? ALPHA-FETOPROTEIN FLEX? REAGENT CARTRIDGE |
Product Code | LOJ |
Date Received | 2019-04-11 |
Catalog Number | K6454 SMN 10463378 |
Lot Number | 18309BE |
Device Expiration Date | 2019-11-05 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SIEMENS HEALTHCARE DIAGNOSTICS INC |
Manufacturer Address | 500 GBC DRIVE P.O. BOS 6101 NEWARK DE 197146101 US 197146101 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-04-11 |