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 2020-03-26 for DIMENSION EXL WITH LOCI MODULE (LM) INSTRUMENT DIMENSION EXL WITH LM 10486890 manufactured by Siemens Healthcare Diagnostics Inc..
Report Number | 2517506-2020-00121 |
MDR Report Key | 9884588 |
Report Source | HEALTH PROFESSIONAL,USER FACI |
Date Received | 2020-03-26 |
Date of Report | 2020-03-26 |
Date of Event | 2020-03-02 |
Date Mfgr Received | 2020-03-02 |
Device Manufacturer Date | 2014-10-20 |
Date Added to Maude | 2020-03-26 |
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 | KARL AEBIG |
Manufacturer Street | 511 BENEDICT AVE |
Manufacturer City | TARRYTOWN, NY |
Manufacturer Country | US |
Manufacturer Phone | 5243102 |
Manufacturer G1 | SIEMENS HEALTHCARE DIAGNOSTICS INC. |
Manufacturer Street | REGISTRATION #: 1226181 101 SILVERMINE ROAD |
Manufacturer City | BROOKFIELD, DE |
Manufacturer Country | US |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | DIMENSION EXL WITH LOCI MODULE (LM) INSTRUMENT |
Generic Name | DIMENSION EXL WITH LOCI MODULE (LM) INSTRUMENT |
Product Code | JJE |
Date Received | 2020-03-26 |
Model Number | DIMENSION EXL WITH LM |
Catalog Number | 10486890 |
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 PO BOX 6101 NEWARK, DE US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-26 |