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 2019-11-18 for ADVIA CENTAUR XPT RUBELLA G (RUB G) N/A 10310283 manufactured by Siemens Healthcare Diagnostics, Inc..
Report Number | 1219913-2019-00237 |
MDR Report Key | 9338726 |
Report Source | HEALTH PROFESSIONAL,USER FACI |
Date Received | 2019-11-18 |
Date of Report | 2019-11-18 |
Date of Event | 2019-10-23 |
Date Mfgr Received | 2019-10-24 |
Device Manufacturer Date | 2019-04-05 |
Date Added to Maude | 2019-11-18 |
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 | MS. STACY LOUKOS |
Manufacturer Street | 333 CONEY STREET |
Manufacturer City | EAST WALPOLE MA 02032 |
Manufacturer Country | US |
Manufacturer Postal | 02032 |
Manufacturer Phone | 5086608576 |
Manufacturer G1 | SIEMENS HEALTHCARE DIAGNOSTICS, INC. |
Manufacturer Street | 333 CONEY STREET |
Manufacturer City | EAST WALPOLE MA 02032 |
Manufacturer Country | US |
Manufacturer Postal Code | 02032 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ADVIA CENTAUR XPT RUBELLA G (RUB G) |
Generic Name | RUBELLA G IMMUNOASSAY, |
Product Code | LFX |
Date Received | 2019-11-18 |
Model Number | N/A |
Catalog Number | 10310283 |
Lot Number | UNKNOWN |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SIEMENS HEALTHCARE DIAGNOSTICS, INC. |
Manufacturer Address | 511 BENEDICT AVENUE TARRYTOWN NY 105915097 US 105915097 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-11-18 |