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 2020-02-25 for BN II SYSTEM 10462274 manufactured by Siemens Healthcare Diagnostics Products Gmbh.
Report Number | 9610806-2020-00008 |
MDR Report Key | 9750205 |
Report Source | FOREIGN,USER FACILITY |
Date Received | 2020-02-25 |
Date of Report | 2020-02-25 |
Date of Event | 2020-01-24 |
Date Mfgr Received | 2020-01-29 |
Date Added to Maude | 2020-02-25 |
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 | CHRISTOPHER AEBIG |
Manufacturer Street | 511 BENEDICT AVE |
Manufacturer City | TARRYTOWN, NY |
Manufacturer Country | US |
Manufacturer Phone | 5242740 |
Manufacturer G1 | BIT ANALYTICAL INSTRUMENTS GMBH |
Manufacturer Street | REGISTRATION NUMBER: 300360107 AM KRONBERGER HANG 3 |
Manufacturer City | SCHWALBACH, 65824 |
Manufacturer Country | GM |
Manufacturer Postal Code | 65824 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | BN II SYSTEM |
Generic Name | BN II SYSTEM |
Product Code | JQX |
Date Received | 2020-02-25 |
Model Number | BN II SYSTEM |
Catalog Number | 10462274 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH |
Manufacturer Address | EMIL-VON-BEHRING- STR. 76 MARBURG, D-35041 GM D-35041 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-02-25 |