CLINITEK ADVANTUS 10484765

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 07 report with the FDA on 2013-07-09 for CLINITEK ADVANTUS 10484765 manufactured by Siemens Healthcare Diagnostics, Inc..

Event Text Entries

[3685774] Customer reported a negative protein results on the instrument but the visual results were positive. There was no report of injury for this event.
Patient Sequence No: 1, Text Type: D, B5


[11038914] The cause for the discordant protein results is unknown.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1217157-2013-00125
MDR Report Key3229823
Report Source07
Date Received2013-07-09
Date of Report2013-06-27
Date of Event2013-06-25
Date Mfgr Received2013-06-27
Date Added to Maude2013-07-22
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 FDA0
Event Location0
Manufacturer ContactSTEVE ANDBERG
Manufacturer Street2 EDGEWATER DR.
Manufacturer CityNORWOOD MA 02062
Manufacturer CountryUS
Manufacturer Postal02062
Manufacturer Phone7812693655
Manufacturer G1KIMBALL ELECRONICS POLAND SP.Z O.O
Manufacturer StreetUL. POZENANSKA 1/C
Manufacturer CityTARNOWO PODGOME 62-08
Manufacturer CountryPL
Manufacturer Postal Code62-08
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCLINITEK ADVANTUS
Generic NameCLINITEK ADVANTUS
Product CodeJIR
Date Received2013-07-09
Catalog Number10484765
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSIEMENS HEALTHCARE DIAGNOSTICS, INC.
Manufacturer AddressTARRYTOWN NY 10591509 US 10591 5097


Patients

Patient NumberTreatmentOutcomeDate
10 2013-07-09

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