» TECHNOCLOT® PT Owren Capillary Control Set

HEMOSTASIS COAGULATION ROUTINE SCREENING TESTS PT APTT FIBRINOGEN TT

TECHNOCLOT® PT Owren Capillary Control Set

Prothrombine Time

TECHNOCLOT® PT Owren Capillary Control Set is used for precision and precise control of capillary blood INR tests.

Consists of a normal freeze-dried plasma and an anticoagulated plasma used to determine the accuracy and accuracy of INR tests.

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Reference	4-5005102
Presentation	Kit
Format	2 x 1.0 mL
Quote

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

Reference	Presentation	Format	Quote	Product sheet
4-5005102	Kit	2 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” pathway of coagulation (factor VII, X,V,II) as well as the conversion of fibrinogen to fibrin.

- A set of normal and anticoagulated freeze-dried plasmas designed to control capillary blood INR tests.
- Normal plasma is prepared from selected citrated plasma from healthy donors so that coagulation activity is normally distributed.
Abnormal plasma is prepared from donor plasma stabilized on long-term warfarin treatment with the same coagulation levels Factors II, VII and X plus PIVKA proteins present in the patient’s plasma.
- TECHNOCLOT® PT Owren Capillary Control Set is used as a supplement to the TECHNOCLOT® PT Owren Manual reagent.

- Simple to use - CaCL2 included in the set.
- Excellent stability once restored.

- 1 vial x 1 mL Capillary Control N
- 1 vial x 1 mL Capillary Control AK
- 2 vials x 1 mL distilled water
- 2 vials x 1 mL CaCl₂

TECHNOCLOT® PT Owren Automated
TECHNOCLOT® PT Owren Capillary Calibration 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