» CRYOcheck™ Abnormal 2 Reference Control

HEMOSTASIS COAGULATION ROUTINE FROZEN CALIBRATORS AND CONTROLS SPECIALTY CONTROLS

CRYOcheck™ Abnormal 2 Reference Control

Fresh frozen plasmas

Ready-to-use pathology control plasma to measure the accuracy of quantitative hemostasis assays.

This specialized quality control is titrated for values in the pathological zone between 5 and 10%. Titrated for the following parameters : Fibrinogen, Factor II, Factor V, Factor VII, Factor VIII (Chromogenic and Clotting), Factor IX, Factor X, Factor XI, Factor XII, Factor XIII, VWF : Ag, Plasmin Inhibitor, PS activity, Free PS and total Ag, AT activity and AT Ag, PC activity and PC Ag, Plasminogen.

Access publications on the manufacturer's website

Reference	ARP2-10
Presentation	Kit
Format	25 x 1.0 mL
Quote

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

Reference	Presentation	Format	Quote	Product sheet
ARP2-10	Kit	25 x 1.0 mL

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

CRYOcheck™ Abnormal 2 Reference Control Certificate of analysis

- Flash freezing under nitrogen
- No bovine additives
- No reconstitution error
- No deterioration of plasmas linked to freeze-drying
- Plasmas verified negative for all tests required by the FDA
- Expiration date of 3 years from the date of manufacture with storage between -40°C and -80°C
- Packaging in plastic cryotubes suitable for all STA-R type microgodets

- Citrate 3.2% equivalent
- Ready to use in minutes after thawing
- Compact, color-coded boxes for easier identification in freezers
- ISTH / SSC international standard
- Certificate of analysis supplied with each batch for 22 parameters

Each parameter of the CRYOcheck™Abnormal 2 Reference Control is titrated for values at the lower limit of the pathological zone around 5 to 10%. Reference values are assigned by independent and internationally recognized laboratories using international reference standards (for existing ones) using different hemostasis analyzers.

- 25 cryotubes x 0.5 mL or 1 mL of frozen plasma

CRYOcheck™ Abnormal 1 Reference Control
CRYOcheck™ Low Fibrinogen Control
CRYOcheck™ Normal Reference Plasma
CRYOcheck™ Reference Control Normal

	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 FROZEN CALIBRATORS AND CONTROLS SPECIALTY CONTROLS