2010 Diagnostica Stago TCoag Destiny Max Coagulation Analyzer Blood Clot testing

This 2010 model year unit was purchased from a hospital near Chicago. The hospital was downsizing and no longer needed it. As a result it has seen very little use. It comes with everything pictured, including a computer, analysis software, almost 300 new covette trays, 5 bottles of system fluid, three extra needles and much more. The unit has a clear history, and is in excellent condition. According to the manufaturer, it was last serviced in June of 2012 and requires annual checkups. While we have taken great pains to make sure the machine is clean and in good working order, we are not qualified technicians and recommend that you order a checkup once it is set up. We would be happy to assist you with that process. If you have questions about this unit please feel free to call us at 419-645-5463! You can view many more pictures on our website. www.industrialmerchants.com Instrument name/First year sold Destiny Max/2009 Country where analyzer designed/Manufactured Germany/Germany Operational type continuous random access Reagent type open reagent system Operates on whole blood or spun plasma spun plasma Sample handling system continuous rack loading Model type benchtop Dimensions (H × W × D)/Weight/Instrument footprint 29.5 × 59 × 27 in/340 lbs/11.03 square feet FDA-cleared clotting-based tests open system: all clottable assays can be run on Destiny Max (PT, PTT, FIB, TT, factors, venom time, proteins C and S, aPCR, lupus screen and confirm) FDA-cleared chromogenic tests open system: all chromogenic assays can be run on Destiny Max (prot C, AT IIa and Xa based), heparin Xa, plasminogen FDA-cleared immunologic tests open system: all latex immunoassays can be run on Destiny Max (D-dimer) Other FDA-cleared tests — User-defined tests in clinical use — Tests submitted for 510(k) clearance — Tests in development but not yet submitted all coagulation tests Methodologies supported clot detection, mechanical and optical; chromogenic; immunologic Operator must load sep. reagent pack per specimen/Test run no/no Number of different measured assays onboard simultaneously unlimited Number of different assays programmed and calib. at one time unlimited Number of user-definable (open) channels unlimited Of those defined, number active simultaneously unlimited Factor assays require manual manipulation or dilutions no Number of reagent containers onboard at once/Tests per container/Reagents refrigerated onboard —/varies by test/yes (12°–16°C) Multiple reagent configurations supported yes Reagents, consumables loaded without interrupting testing yes Same capabilities when third-party reagent used no Maximum time same lot number of reagents can be used varies—routine reagents 12 months Walkaway capacity: Number of specimens/Number of tests 120/71,000 Minimum sample volume aspirated precisely at one time 25 µL Standard specimen volume required to run PT or PTT/ Factor VIII activity 25 µL/10 µL Disposables used/Price of each reaction trays, ProWash Supports direct-from-track sampling yes Primary tube sampling supported/Pierces caps on primary tubes yes/yes Sample bar-code reading capability yes/yes Reagent bar-code reading capability yes Onboard test automatic inventory yes Measures No. of tests remaining/Short sample detection yes/yes Clot detection as preanalytical variable in plasma sample no Auto. detects adequate reagents for aspiration and analysis yes Hemolysis/Turbidity detection-quantitation not necessary/not necessary Dilution of patient samples onboard yes Automatic rerun capability/Auto reflex testing capability yes/yes Lag time during which hypercoagulable sample not detected no Read time extended for prolonged clotting times yes User can set different-than-standard:   • Reagent volumes/Sample volumes yes/yes • No. and sources of reagent yes • Incubation times/Reading times yes/yes Autocalib. or autocalib. alert/Multipoint calib. supported yes/yes Auto shutdown/Auto startup programmable yes/yes Stat time to complete all analytes/Throughput per hour for:   • PT alone • PT, PTT • Fibrinogen • Factor VIII activity assay Time delay from ordering stat to aspiration of sample Automatic transfer of QC results to LIS yes Data-management capability onboard (includes QC: L-J plots, Westgard Multirules) Interface supplied by instrument vendor no Interfaces in active user sites for: — Bidirectional interface capability yes (broadcast download and host query) Results transferred to LIS as soon as test time complete yes LOINC codes transmitted with all results no How labs get LOINC codes for reagent kits package insert, e-mail Electronic interface available (or will be) to automated (or robotic) specimen handling system yes Modem servicing yes Time required for maintenance by lab personnel daily: Onboard maintenance records yes     Approximate number of training hours needed per tech  5 List price   $134,160     Distinguishing features (supplied by company) mechanical and optical clot detection; closed tube sampling; dyes in routine reagents for volume delivery check; factor parallelism; normalization of PT and PTT results; LAS ready