SURECAN SAFETY II 4447051-02

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-03-16 for SURECAN SAFETY II 4447051-02 manufactured by B. Braun Medical France.

MAUDE Entry Details

Report Number9612452-2020-00009
MDR Report Key9834547
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-03-16
Date of Report2020-03-16
Date of Event2020-02-18
Date Mfgr Received2020-02-18
Device Manufacturer Date2017-11-04
Date Added to Maude2020-03-16
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 ContactMR. JONATHAN SEVERINO
Manufacturer Street861 MARCON BLVD.
Manufacturer CityALLENTOWN, PA
Manufacturer CountryUS
Manufacturer Phone2408332
Manufacturer G1B. BRAUN MEDICAL FRANCE
Manufacturer Street30 AVENUE DES TEMPS MODERNES
Manufacturer City86360
Manufacturer CountryFR
Manufacturer Postal Code86360
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSURECAN SAFETY II
Generic NameNON-CORING (HUBER) NEEDLE
Product CodePTI
Date Received2020-03-16
Model Number4447051-02
Catalog Number4447051-02
Lot Number17M04G8671
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerB. BRAUN MEDICAL FRANCE
Manufacturer Address30 AVENUE DES TEMPS MODERNES 86360 FR 86360


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-16

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