CoaguChek® systems

    The smart way to test INR at the Point of Need

CoaguChek Pro II

CoaguChek Pro II

Make confident treatment decisions at all points of care


The CoaguChek Pro II Coagulation meter features multiple enhancements to the previous generation of CoaguChek devices (CoaguChek XS Plus and CoaguChek XS Pro). It brings the lab closer to the patient in the hospital environment. In addition, it continues to support Vitamin K Antagonist (VKA) therapy monitoring in the professional segments, such as anticoagulation (AC) clinics and GP surgeries.

The CoaguChek Pro II system is used for the determination of PT by healthcare professionals in a Point of Care environment.

In addition to INR monitoring, testing T in critical care situations helps to:

  • Assess coagulation status in bleeding patients or for those taking vitamin K antagonists in A&E
  • Assess vitamin K deficiency, monitor bleeding risk, manage haemostasis and guide transfusion therapy in the operating room
  • Assess vitamin K status and/or vitamin K deficiency in the ICU


Wireless Technology

  • Built in Wifi means that results can be automatically shared among clinicians, nurses and patients for convenient access and delivery
  • No need to dock meter to transmit results
  • Integrated 1d and 2d barcode scanner to capture Operator and Patient IDs
  • QR code feature enables data transmission to any data management system immediately, with no need to transcribe results for a streamlined workflow


Easy to impement with little training

  • The enhanced features of CoaguChek Pro II are simple to use, especially if you've already been using the CoaguChek XS Pro or CoaguChek XS Plus
  • Intuitive user interface makes CoaguChek Pro II easy to use and easy to train


Institution-wide implementation may lead to:

  • Decreased turnaround time
  • Cost savings
  • Streamlined workflow
  • Reduced time to discharge
  • Time savings for staff







Get immediately actionable results
at ALL points of care







System components


The CoaguChek® Pro II meter kit contains:

  • 1 CoaguChek Pro II meter
  • 1 handheld power supply unit
  • 1 user manual in English
  • 1 CD-ROM with other languages: German, French, Italian, English, Spanish, Portuguese, Danish, Norwegian, Swedish, Finnish and Dutch

Optional accessories

  • Handheld base unit kit: docking station (to recharge the battery pack and transfer data to a computer)

Additional required components

  • CoaguChek PT Test strips
    Box with 2 vials of 24 strips with a code chip
  • CoaguChek PT Controls
    4 vials of level 1 control
    4 vials of level 2 control
    8 diluent-filled droppers
    1 code chip


Technical specifications


Measuring & Sampling

Detection system
- PT: Amperometric (electrochemical) determination  after activation of the blood coagulation with human recombinant thromboplastin

User interface
Full graphical (TFT)

Support and safety functions
2D Barcode Scanner, QC lockout, Patient & User ID, protection with administrator ID.

Sample application
Outside the meter, with top and side (left or right)-dosing options

Operating Conditions

Operating Temperature
+12° C to +32 °C (54 °F to 90 °F)

Operating humidity and altitude
10 - 85% - 4300 m (14,000 ft)

Operate the meter on a level, vibration free surface, or hold it so that it is roughly horizontal.

Measuring range
- PT/INR: 0.8 - 8.0; %Q: 120 - 5; SEC: 9.6 – 96

- 2000 patient and 500 QC results with date and time.
- 120 code chip records (60 strip code & 60 control codes)
- Operator list with up to 5000 Operator IDs with corresponding 2nd ID. e.g. operator name
- Patient list with up to 4000 Patient IDs with corresponding 2nd and 3rd patient IDs. e.g name, date of birth

Touch screen and bar code scanner

Power options
- Universal battery pack for the CoaguChek Pro II
- Power supply adapter: input: 100-240 V / 50-60Hz / 350 - 150 mA; output: 12 V DC/ 1.25 A

Number of tests w/ fully charged battery pack
- Approx. 60 tests - PT/INR

187 x 97 x 43 mm

280 g (without batteries)

Safety Class

Auto power off
Programmable 1 to 60 minutes

Sample Material

Sample type
Capillary, venous, or arterial fresh whole blood

Sample size
≥ 8 µl

Refer to the test strip package insert

Test Strips

Approx. 1.0

Sensitivity to heparin
- PT/INR: Insensitive to unfractionated and fractionated heparin concentrations up to 3 IU/mL blood

Quality control
On each strip, through the same channel as the blood passes

Store at + 2° C to + 30° C. Test strips can be used until expiry date printed on the box and test strip vial.