{ "ProductData": { "RelatedLinks": "", "RegulatoryDisclaimer1": "", "RegulatoryDisclaimer2": "", "StainLocalization": [ "" ], "ProductType": "Instrument", "DisclaimerGroup2": null, "ProductNameGlobal": "CoaguChek Vantus", "DisclaimerGroup1": null, "ControlTissue": [ "" ], "BrandName": "CoaguChek^® Vantus", "LicenseDisclaimers": [ ], "Isotypes": "", "RegulatoryDisclaimer3": "", "ID": "INS_6269", "ProductNameAddition": "", "Species": [ "" ], "Clone": "" }, "ProductImageDetails": { "ImagePath": "https://pim-media.roche.com/Images/qCoagucheckVantus.png", "ImageType": "Image main" }, "Product2Taxomony": { "Product2TaxomonyReferences": [ { "StructureSystemIdentifier": "1", "StructureSystemName": "GPCH", "NodeName": "CoaguChek Vantus", "NodeID": "9423" }, { "StructureSystemIdentifier": "OWP_Organization", "StructureSystemName": "Organization", "NodeName": "Coagulation, Hematology and Urinalysis", "NodeID": "10-10-20-30-00" }, { "StructureSystemIdentifier": "OWP_Product_Solutions", "StructureSystemName": "OWP Product Solutions", "NodeName": "Point of Care", "NodeID": "110" }, { "StructureSystemIdentifier": "OWP_Family", "StructureSystemName": "Product Families", "NodeName": "CoaguChek", "NodeID": "090" }, { "StructureSystemIdentifier": "OWP_Product_Types", "StructureSystemName": "Product Types", "NodeName": "Analyzer Instruments and Systems", "NodeID": "10-000-00" }, { "StructureSystemIdentifier": "Lab_Type", "StructureSystemName": "Lab Types", "NodeName": "Point of Care Testing", "NodeID": "110-00" }, { "StructureSystemIdentifier": "Product_Solutions", "StructureSystemName": "Product Solutions", "NodeName": "Coagulation", "NodeID": "070" }, { "StructureSystemIdentifier": "Disease_Areas", "StructureSystemName": "Disease Areas", "NodeName": "Coagulation Monitoring", "NodeID": "10-00-00" }, { "StructureSystemIdentifier": "OWP_Techniques", "StructureSystemName": "Techniques", "NodeName": "NOT APPLICABLE", "NodeID": "999-00" }, { "StructureSystemIdentifier": "Pathogens", "StructureSystemName": "Pathogens", "NodeName": "NOT APPLICABLE", "NodeID": "99-00-00" }, { "StructureSystemIdentifier": "Applications", "StructureSystemName": "Applications", "NodeName": "NOT APPLICABLE", "NodeID": "99-00-00" }, { "StructureSystemIdentifier": "Health_Topics", "StructureSystemName": "Health Topics", "NodeName": "NOT APPLICABLE", "NodeID": "99-00-00" }, { "StructureSystemIdentifier": "Health_Topics", "StructureSystemName": "Health Topics", "NodeName": "Critical Care", "NodeID": "11-00-00" } ] }, "Product2Materials": { "P2MaterialReferences": [ { "MaterialNum": "07729952160", "MaterialDescription": "CoaguChek Vantus (USA)", "RegisteredProductName": "CoaguChek® INRange", "GTIN": "00365702700499", "ProductCategoryText": "Meters", "OldMaterialNumber": "", "PackSizePIM360": "", "PackSizeDescPIM360": "", "MaterialAnnotation": "", "ReadyForUse": "", "OrderInformation": "" } ] }, "Product2Products": { "Product2ProductReference": [ ] }, "ProductSpec": [ { "ProductSpecVariant": { "Chapters": [ { "Language": "en", "Value": "The CoaguChek^® Vantus System measures an INR (International Normalized Ratio) based on a prothrombin time (PT) response to monitor the effect of a therapy with vitamin K antagonists by using the CoaguChek XS^® PT Test strips. The CoaguChek Vantus System uses fresh capillary whole blood from a finger stick.

The system is intended for properly selected and suitable trained users on the prescription of the treating doctor. Users should be stabilized on anticoagulation with vitamin K antagonists for at least 6 weeks prior to single patient self-testing with the CoaguChek Vantus System.

The CoaguChek Vantus System is intended for single patient self-testing only for adults, age 22 years and older.", "Name": "Intended Use" } ] } } ] }

CoaguChek^{^®} Vantus

The future of INR self-testing

Trust in your patients’ self-testing results like never before. Accurate INR results are transmitted wirelessly via Bluetooth®-enabled CoaguChek Vantus and can help improve patient compliance versus clinic-based testing, which may increase time in therapeutic range (TTR), and enable therapy decisions based on current results.^1,2,3

A new standard of technology for warfarin patients:
Easy to use. The CoaguChek Vantus is designed with features to make accurate self-testing as easy and as repeatable as possible, including full-color display with easy-to-use on-screen instructions.

Minimal pain. The CoaguChek XS Softclix Lancing Device is a specially designed lancing device that pricks the skin with a lancet to obtain just one drop of blood for testing.

Simplified patient experience. IDTF partners facilitate data result transfer and testing reminders, and make it easy to test from the comfort of your own home.

Seamless transfer of INR test results. With the CoaguChek Vantus, no phone calls are needed and no manual entry on a web page is required. The results can be accurately reported via Bluetooth connectivity.

Product support. If you or your patients have product related questions, live technical support is available by phone at 1-800-428-4674.

Do you have any questions?

References

Bluetooth connectivity requires a smartphone or tablet. Minimum specifications required.
Kortke, H., Minami, K., Reymann, T., et al., (2001). “INR self-management after mechanical heart valve replacement: ESCAT (Early Self-Controlled Anticoagulation Trial).” Z Kardiol 90(6)118-124.
Heneghan C, Alonso-Coello P, Garcia-Alamino JM, Meats E and Glasziou P. Self-monitoring of oral anticoagulation: a systematic review and meta-analysis. Lancet. 2006;367:404-411

Call 1-800-780-0675 for a list of supported devices and operating systems.