» TECHNOCLOT® PT Owren Capillary Calibration Set

HEMOSTASIS COAGULATION ROUTINE SCREENING TESTS PT APTT FIBRINOGEN TT

TECHNOCLOT® PT Owren Capillary Calibration Set

Prothrombine Time

TECHNOCLOT® PT Owren Capillary Calibration set is used to establish an INR Reference curve for capillary blood INR tests.

A set of 4 freeze-dried calibration plasmas for standardisation and calibration of INR capillary blood tests using TECHNOCLOT® PT Owren Manual.

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Reference	4-5005100
Presentation	Kit
Format	4 x 1.0 mL
Quote

Price list, safety data sheets and notices are accessible to our registered customers.

Reference	Presentation	Format	Quote	Product sheet
4-5005100	Kit	4 x 1.0 mL

Price list, safety data sheets and notices are accessible to our registered customers.

Prothrombin time is the measurement of the clotting time of citrate plasma by adding an excess of calcium tissue thromboplastin.
The test explores the “extrinsic” route of coagulation (factor VII, X,V,II) as well as the conversion of fibrinogen to fibrin.

Set contains both a normal and 3 warfarinised plasmas with calibrated INR values.
TECHNOCLOT® PT Owren Capillary Calibration Set est utilisé en complément du réactif TECHNOCLOT® PT Owren Manual.

- Simple to use - CaCL2 and distilled water included in the set
- INR's of patient samples can be direct read off from the calibration curve
- Suitable for use with TECHNOCLOT® PT Owren Manual and other PT systems

- 1 vial of 1 mL of lyophilised normal plasma
- 3 vials of 1 mL of lyophilised anticoagulated plasma with calibrated INR values
- 4 vials of 1 mL of distilled water
- 4 vials of 1 mL of CaCl₂

TECHNOCLOT® PT Owren Automated
TECHNOCLOT® PT Owren Capillary Control Set
TECHNOCLOT® PT Owren Manual

	These kits are manufactured in accordance with the 98/79 EC directive for in vitro diagnostic devices. Only CE marked products can be used for diagnostic applications in Europe.
	These kits are intended for in vitro diagnostic use.
	These kits are for research use only and are not intended to be used for diagnostic procedures.
	Federal Drug Administration, FDA validates diagnostic kits for in vitro diagnostic use in the United States.
	Biological risk products.
	Storage between 2 and 8 ° C.
	Reactive in liquid form.
	Reactive in lyophilized form.
	Reactive in frozen form.
	Stability after opening at 2-8 ° C.
	Products that can be refrozen.
	Stability 12 months after refreezing at -20 ° C.
	Manufacturer.
	Importer
	Distributor.

HEMOSTASIS COAGULATION ROUTINE SCREENING TESTS PT APTT FIBRINOGEN TT