BN II SYSTEM 10462274

MAUDE Adverse Event Report

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 2020-02-10 for BN II SYSTEM 10462274 manufactured by Siemens Healthcare Diagnostics Products Gmbh.

MAUDE Entry Details

Report Number9610806-2020-00005
MDR Report Key9688437
Report SourceFOREIGN,USER FACILITY
Date Received2020-02-10
Date of Report2020-02-10
Date of Event2019-12-13
Date Mfgr Received2020-01-13
Date Added to Maude2020-02-10
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactCHRISTOPHER AEBIG
Manufacturer Street511 BENEDICT AVE
Manufacturer CityTARRYTOWN, NY
Manufacturer CountryUS
Manufacturer Phone5242740
Manufacturer G1BIT ANALYTICAL INSTRUMENTS GMBH
Manufacturer StreetREGISTRATION NUMBER: 300360107 AM KRONBERGER HANG 3
Manufacturer CitySCHWALBACH, 65824
Manufacturer CountryGM
Manufacturer Postal Code65824
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBN II SYSTEM
Generic NameBN II SYSTEM
Product CodeJQX
Date Received2020-02-10
Model NumberBN II SYSTEM
Catalog Number10462274
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
Manufacturer AddressEMIL-VON-BEHRING- STR. 76 MARBURG, D-35041 GM D-35041


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-10

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.