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Hemochron Elite - Itc Usa

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New Compliance Technology

The Complete Solution to Ease


The HEMOCHRON Signature Elite® is a simple, easy-to-use, portable
microcoagulation system that enhances compliance and patient safety.
With HEMOCHRON systems’ extensive test menu you can standardize
your point-of-care (POC) coagulation testing throughout your facility.

Improves Safety and Security


• I ntegrated barcode scanner can eliminate
transcription errors
• Ability to scan cuvette and QC lot
information, patient identification (PID)
and operator ID (OID)
• Barcode technology provides audit trail
and traceability
Enhances Compliance
• A utomatic internal electronic quality control (EQC)
• Quality control (QC) lockout including cuvette
and QC expiration lockout
• Operator certification tracking and lockout

Integrates Data Management/Connectivity


• Direct connection to Ethernet
• POCT-1A compliant device meets industry standard
• Connectivity to major information systems
• Configurable settings provide flexibility

Simplifies Testing
• S imple, standardized test procedure reduces user variability
• No measuring or sample preparation required
• Easy to train the operators and easy to learn
• Easy to read, large display screen
Your Compliance Challenges

AC/DC Power Port

Port to
Connect
Computer or
Printer

Ethernet Port
Broad Testing Menu
• U tilizes microcoagulation technology that measures the actual endpoint of thrombosis which is clot formation
• Provides a comprehensive test menu to meet needs throughout your facility
Test include:
ACT+
ACT-Low Range
PT
APTT
Citrate PT
Citrate APTT
*HEMONOX ™

Cuvette Intended Use Specimen Reporting Unit


ACT-LR Monitors low to moderate heparin doses up to 2.5 units/mL Whole blood Celite Equivalent Seconds
of blood.
Used in procedures such as cardiac catherization,
Extracorporeal Membrane Oxygenation (ECMO), dialysis and
Pertaneous Transluminal Cornary Angioplasty.

ACT+ Monitors moderate to high levels of heparin (1-6 units/mL). Whole blood Celite Equivalent Seconds
Unaffected by aprotinin, hypothermia, and hemodilution.

pT For performing a quantitative, one-stage prothrombin time. Venous or International Normalized


fingerstick Ratio (INR), plasma-equivalent
samples seconds and whole blood
seconds
citrate PT For performing a quantitative, one-stage prothrombin time. Citrated International Normalized
whole blood Ratio (INR), plasma-equivalent
seconds and whole blood
seconds
APTT For performing a quantitative, one-stage APTT. For evaluation of Whole blood Plasma equivalent units up to
low dose heparin anticoagulation (up to 1.5 units/mL of blood). 400 seconds and whole blood
seconds
citrate APTT For performing a quantitative, one-stage APTT. For evaluation of Citrated Plasma equivalent units up to
low dose heparin anticoagulation (up to 1.5 units/mL of blood). whole blood 400 seconds and whole blood
seconds
HEMONOX To monitor the anticoagulant effect of enoxaparin sodium Whole blood Whole blood seconds
and dalteparin sodium in patient samples of fresh whole
blood. The HEMONOX assay provides the ability to monitor
the anticoagulant effect through the measurement of the
prolongation of clotting time in response to the presence of
enoxaparin sodium or dalteparin sodium.

For more information contact us at 1-800-631-5945 or visit www.itcmed.com

* HEMONOX is not commercially available in the United States or Canada


ITC, HEMOCHRON and HEMOCHRON Signature Elite are registered trademark of
International Technidyne Corporation in the United States and other jurisdictions.
Celite is a registered trademark of Celite Corporation.

International Technidyne Corporation


8 Olsen Avenue • Edison, NJ 08820 USA
tel: 732.548.5700 • fax: 732.248.1928
www.itcmed.com
a subsidiary of Thoratec Corporation
MSIG:179 7/07

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