» TECHNOCLOT® PT Owren Manual

HEMOSTASIS COAGULATION ROUTINE SCREENING TESTS PT APTT FIBRINOGEN TT

TECHNOCLOT® PT Owren Manual

Prothrombine Time

TECHNOCLOT® PT Owren manual is a thromboplastin reagent for the quantitative determination of prothrombin time (PT) in citrated human plasma, capillary blood and venous blood.

This reagent is sensitive to abnormal levels of coagulation factors II, VII and X.
It is used for the control of blood clotting disorders of the extrinsic system as well as for monitoring oral anticoagulant therapy (i.e. warfarin).

To view a YouTube video presentation about TECHNOCLOT® PT Owren please use the link.

Reference	4-5005037
Presentation	Kit
Format	10 x 10 mL
Quote

Reference	4-5005032
Presentation	Kit
Format	10 x 4.0 mL
Quote

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

Reference	Presentation	Format	Quote	Product sheet
4-5005037	Kit	10 x 10 mL
4-5005032	Kit	10 x 4.0 mL

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

Prothrombin time (PT) is a measure of the clotting time of citrated plasma by addition of excess calcium tissue thromboplastin.
The test explores the “extrinsic” pathway of coagulation (factor VII, X, V, II) as well as the conversion of fibrinogen into fibrin.

TECHNOCLOT® PT Owren manual is specially designed for use with manual methods and semi-automated coagulometers.
The reagent is lyophilized and contains rabbit brain thromboplastin and adsorbed bovine plasma.
The adsorbed plasma is added as a source of factor V and fibrinogen.

- Combined thromboplastin that already contains CaCl2.
- TECHNOCLOT® PT Owren manuel was compared in studies to other reagents on the market and shows very good correlation data.

- 10 vials x 4 or 10 mL

AK Verification Kit
AK-Calibrant
Coagulation Control A
Coagulation Control AK
Coagulation Control N
Coagulation Reference
TECHNOCLOT® PT Owren Capillary Calibration Set
TECHNOCLOT® PT Owren Capillary Control Set

	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