» TECHNOPLASTIN® HIS

HEMOSTASIS COAGULATION ROUTINE SCREENING TESTS PT APTT FIBRINOGEN TT

TECHNOPLASTIN® HIS

Chronometric assay

Thromboplastin calcium for the determination of prothrombin (PT), prothrombin time (PT) and INR (ISI around 1.2).

TECHNOPLASTIN® HIS (HIS = Heparin InSensitive) is a routine hemostasis test composed of standard thromboplastin calcium based on rabbit brain.

Access on the manufacturer's website TECHNOCLONE

Reference	4-5003009
Presentation	Vial
Format	12 x 2.0 mL
Quote

Reference	4-5003021
Presentation	Vial
Format	20 x 10.0 mL
Quote

Reference	4-5003026
Presentation	Vial
Format	6 x 10.0 mL
Quote

Reference	4-5003030
Presentation	Vial
Format	2 x 10,0 mL
Quote

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

Reference	Presentation	Format
4-5003009	Vial	12 x 2.0 mL
4-5003021	Vial	20 x 10.0 mL
4-5003026	Vial	6 x 10.0 mL
4-5003030	Vial	2 x 10,0 mL

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

Prothrombin Time (PT) is the measurement of the clotting time of citrate plasma by the addition of excess calcium tissue thromboplastin.
The test explores the “extrinsic” coagulation pathway (factor VII, X,V,II) and the conversion of fibrinogen to fibrin.

This reagent is characterized by its sensitivity to FII, FV, FVII and FX. It also contains a heparin neutralizer which allows the determination of the PT in the plasmas of patients under conventional heparin therapy (0.2 to 0.8 IU / mL).
This screening test is used for :

- control of coagulation disorders of the extrinsic pathway,
- control of oral anticoagulation therapy,
- the determination of the individual factors of the extrinsic pathway,
- checking the synthesis capacity of coagulation factors in the event of liver disease.

Therapeutic range of oral anticoagulants : INR 2.0 - 4.5 equivalent to 20 - 45% of the norm.

AK-Calibrant
Coagulation Control A
Coagulation Control AK
Coagulation Control N
Coagulation Reference
TECHNOCLOT® Control A
TECHNOCLOT® Control N

	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