Triage Meter Pro User Manual



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Manufacturer of the i-STAT System, a handheld blood analyzer for point-of-care testing, and the US distributor for Piccolo Xpress. Page 73 User ID Main Menu Recall Results ® To retrieve results from tests run on the Alere Triage MeterPro starting with the user you Misc. Test Results select. Press the key to power the Alere Triage ® MeterPro on. Thermoteknix FevIR Scan 2 System is an adjunctive diagnostic screening system, fully compliant as an approved device, within the FDA Enforcement Policy for Telethermographic Systems during the Coronavirus Disease 2019 (COVID-19) Public Health Emergency: Docket Number: FDA-2020-D-1138. METER, TRIAGE METERPRO FLUORESCENCE BD/S. Rapid easy to use technology with a convenient user interface to aid in fast and accurate diagnosis of critical diseases The Triage Meterpro is a portable, rapid testing platform designed to provide rapid, quantitative or qualitative results.

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Triage Meter Pro User ManualBiosite triage meter pro manual
ALERE SAN DIEGO, INC. TRIAGE METER PRO CARDIAC MARKER TESTBack to Search Results
Model Number 52111
Device Problems Power Cord (497); Smoking (1585); Device Inoperable (1663)
Patient Problem No Consequences Or Impact To Patient (2199)
Event Date 02/11/2011
Event Type Malfunction
Event Description

Caller reports power cord to triage barcode scanner was visibly smoking and no longer works. No surges in electricity were observed on site. No explanations for cord damage were offered or source of ignition were found. No personnel were injured or hurt on site. A replacement barcode kit was sent to the customer. Part #52111 corresponds to the replacement barcode kit, which includes the barcode reader and all of its individual accessories. The part number for the triage meter pro is (b)(4).

Manufacturer Narrative

Investigation pending.

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Alere Triage Meter User Manual

Type of DeviceCARDIAC MARKER TEST
Manufacturer (Section D)
ALERE SAN DIEGO, INC.
san diego CA
Manufacturer Contact
carmen bergelin, manager
9975 summers ridge road
san diego, CA 92121
8588052256
MDR Report Key2047391
MDR Text Key19272143
Report Number2027969-2011-00476
Device Sequence Number1
Product Code KHO
Combination Product (Y/N)N
Reporter Country CodeUS
PMA/PMN NumberK973547
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source TypeOther,Health Professional
Reporter Occupation NOT APPLICABLE
Type of ReportInitial
Report Date03/10/2011
1 Device Was Involved in the Event
0 PatientS WERE Involved in the Event:
Date FDA Received03/10/2011
Is This An Adverse Event Report? No
Is This A Product Problem Report? Yes
Device Operator HEALTH PROFESSIONAL
Device MODEL Number52111
Was Device Available For Evaluation? No
Is The Reporter A Health Professional? Yes
Date Manufacturer Received02/11/2011
Was Device Evaluated By Manufacturer? Device Not Returned To Manufacturer
Is The Device Single Use? Yes
Is this a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Unkown