MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-08-27 for SYMBIA EVO EXCEL 10910501 manufactured by Siemens Medical Solutions Usa, Inc..
Report Number | 1423253-2019-00006 |
MDR Report Key | 8936082 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2019-08-27 |
Date of Report | 2019-08-12 |
Date of Event | 2019-08-12 |
Date Mfgr Received | 2019-08-14 |
Device Manufacturer Date | 2019-01-28 |
Date Added to Maude | 2019-08-27 |
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 | LAURA MEYER |
Manufacturer Street | 2501 N. BARRINGTON RD. |
Manufacturer City | HOFFMAN ESTATES IL 60192 |
Manufacturer Country | US |
Manufacturer Postal | 60192 |
Manufacturer Phone | 8472172734 |
Manufacturer G1 | SIEMENS MEDICAL SOLUTIONS USA, INC. |
Manufacturer Street | 2501 N. BARRINGTON RD. |
Manufacturer City | HOFFMAN ESTATES IL 60192 |
Manufacturer Country | US |
Manufacturer Postal Code | 60192 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | SYMBIA EVO EXCEL |
Generic Name | GAMMA CAMERA |
Product Code | KPS |
Date Received | 2019-08-27 |
Model Number | 10910501 |
Device Availability | Y |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SIEMENS MEDICAL SOLUTIONS USA, INC. |
Manufacturer Address | 2501 N. BARRINGTON RD. HOFFMAN ESTATES IL 60192 US 60192 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2019-08-27 |