RAPIDLYTE 3 ML L/S SYRINGE FILTER CAP 10707031

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-07-05 for RAPIDLYTE 3 ML L/S SYRINGE FILTER CAP 10707031 manufactured by Siemens Healthcare Diagnostics.

MAUDE Entry Details

Report Number3002637618-2019-00077
MDR Report Key8764885
Date Received2019-07-05
Date of Report2019-11-22
Date of Event2019-06-11
Date Mfgr Received2019-11-22
Date Added to Maude2019-07-05
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactFELIX AKINRINOLA
Manufacturer Street2 EDGEWATER DRIVE
Manufacturer CityNORWOOD MA 02062
Manufacturer CountryUS
Manufacturer Postal02062
Manufacturer Phone6107052212
Manufacturer G1SMITHS MEDICAL ASD, INC.
Manufacturer Street10 BOWMAN DR.
Manufacturer CityKEENE NH 03431
Manufacturer CountryUS
Manufacturer Postal Code03431
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameRAPIDLYTE 3 ML L/S SYRINGE FILTER CAP
Generic NameRAPIDLYTE 3 ML L/S SYRINGE FILTER CAP
Product CodeGIO
Date Received2019-07-05
Catalog Number10707031
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerSIEMENS HEALTHCARE DIAGNOSTICS
Manufacturer Address511 BENEDICT AVENUE TARRYTOWN NY 10591 US 10591


Patients

Patient NumberTreatmentOutcomeDate
10 2019-07-05

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