official distributor for Bulgaria

Stratus® CS Acute Care™ Troponin Analyzer

The Stratus® CS Analyzer for acute care diagnostics provides quantitative cardiac assays for fast, accurate evaluation of patients presenting with suspected myocardial ischemia. Its efficiency and ease of use make it ideal for both point-of-care testing and lab applications.
  • Easy to use and ideal for all skill levels
  • Full cardiac menu including guideline acceptable troponin I and
    D-dimer (with pulmonary embolism exclusion) assays
  • Results in as little as 14 minutes
  • Use in the acute care setting to decrease turnaround time, patient length of stay, and total patient costs

Managing Chest Pain to Meet the Challenge

Each year, more than eight million patients visit emergency departments in the United States with chest pain suggestive of myocardial ischemia. Yet, in around 75% of cases, objective evidence of unstable coronary syndrome is lacking after the initial clinical and ECG evaluation.

Accelerated diagnostic protocols using biochemical markers and near-patient testing strategies with the Stratus® CS analyzer can help address this challenge. Consequently, hospital stays—and the cost to manage both ACS-positive and ACS-negative patients—can be reduced.

Fast, informative results

  • Rapid turnaround time: 14 minutes to first result, and 4 minutes for each subsequent result
  • A broad menu of tests to support better chest pain differentiation from a single sample, on a single run, on a single instrument 

Easy-to-use in the Emergency Department, Coronary Care Unit,
STAT Lab or Central Lab

  • Simple operation for all skill levels: load sample, rotor, TestPak™ Cartridge(s)—and press Start
  • System accepts blood directly from collection tube—no sample preparation, no manual dilutions
  • Integrated centrifuge spins whole blood to plasma and automatically pipettes to test cartridges—no user manipulation needed

Efficient and cost-effective

  • Eliminates manual intervention steps that prolong result turnaround
  • Single use packaging for tests, calibrators, and diluents reduce reagent waste
  • Select tests based on patient need—no fixed assay panels
  • System Check (electronic QC) reduces liquid QC frequency requirements

Compliant

  • Barcode readers and lockout features for near-patient testing compliance
  • Fully compliant with OSHA Bloodborne Pathogens Preamble
  • First to the market with a guideline acceptable troponin I assay with the low end precision to meet the 2012 ESC/ACC Guidelines

Extensive Support

  • Onsite training
  • Field service group
  • Technical telephone support

Troponin-l

 

Assay Range

0.03 – 50 ng/mL

Sensitivity

<0.03 ng/mL

Reproducibility (CV)

10% at 0.06 ng/mL

Calibration Stability

60 days

DilPak™ Automatic Dilution

Yes

Sodium Heparin Tubes

Yes

Lithium Heparin Tubes

Yes

βhCG

 

Assay Range

0.3 – 150ng/mL (µg/L)

Sensitivity

0.3 ng/mL

Reproducibility (CV)

4.0% at 3.7 ng/mL

Calibration Stability

60 days

DilPak™ Automatic Dilution

Yes

Sodium Heparin Tubes

Yes

Lithium Heparin Tubes

Yes

Myoglobin

 

Assay Range

1 – 900 ng/mL (µg/L)

Sensitivity

1.0 ng/mL

Reproducibility (CV)

3.4% at 56 ng/mL

Calibration Stability

60 days

DilPak™ Automatic Dilution

Yes

Sodium Heparin Tubes

Yes

Lithium Heparin Tubes

Yes

NT-proBNP

 

Assay Range

15 – 20,000 pg/mL

Sensitivity

15.0 pg/mL

Reproducibility (CV)

4.4% at 96.6 pg/mL

Calibration Stability

30 days

DilPak™ Automatic Dilution

Yes

Sodium Heparin Tubes

Yes

Lithium Heparin Tubes

Yes

D-dimer

 

Assay Range

6 – 5000 ng/mL (µg/L) FEU

Sensitivity

6 ng/mL FEU

Precision (CV)

4.1% at 412 ng/mL

Calibration Stability

60 days

DilPak™ Automatic Dilution

Yes

Sodium Heparin Tubes

Yes

Lithium Heparin Tubes

Yes

hs-CRP

 

Assay Range

0.1 – 50 mg/L

Sensitivity

0.10 mg/L

Reproducibility (CV)

6.8% at 1.16 mg/L

Calibration Stability

60 days

Sodium Heparin Tubes

Yes

Lithium Heparin Tubes

Yes

βhCG

 

Assay Range

0.5 – 1,250 mlU/mL (IU/L)

Sensitivity

0.5 mlU/mL

Reproducibility (CV)

2.5% at 27.1 mlU/mL*

Calibration Stability

90 days

DilPak™ Automatic Dilution

Yes

Sodium Heparin Tubes

Yes

Lithium Heparin Tubes

Yes

Automatic Alignment

Level-sensing capabilities automatically align to each TestPak and module

Computer Interface Specifications

Uni-directional through serial port

Environmental Specifications

Room Temperature:

15-30°C (65-85°F)

Humidity:

20–80%

Waste Disposal

All hazardous materials are contained within a disposable waste liner

Centrifuge Speed

Microprocessor-verified between 18,000 and 22,000 rpm

Sample and TestPak Identification

Universal bar code reader

Reagent Capacity

Single-use assay cartridges

Assay Technology

Dendrimer enhanced radial partition immunoassay

Quality Control

Daily system check (electronic QC) with programmable time lockout

Liquid controls are processed after calibration, upon receipt of a previously calibrated lot of reagents or whenever the
site wishes to verify performance, and according to local, state, and/or federal regulations

On-board “QC Required” alert for a time element and/ or range check

Software Features

The last 20 results are stored and can be reprinted and/or transmitted to LIS

Patient ID and/or sample ID entry Sample collection time entry

Unauthorized operator lockout capability

TestPak lot expiration notification

Password protection of advanced setup functions

Reagent Storage Requirements

TestPaks, CalPaks, and DilPaks: 2 to 8°C (Troponin-I CalPak and NT-proBNP CalPak: -10 to -20°C)

Why Choose Us

We believe that success is achieved with professionalism, integrity and perfect teamwork, built on the high moral values of our employees.
Our policy is based on impeccable planning, control and execution, through which we achieve maximum satisfaction of our customers.

Professional
customer service

A wide range of laboratory analyzers

Trained and experienced specialists

Certificate
ISO 13485:2012