Product Comparison


  Sekisui Diagnostics 1039

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LumiraDx Inc L001000330001 Cue Health Inc C0201 Abbott Rapid Dx North America LLC LFR124
McKesson # 1149142 1202548 1198202 1219993 1087252
Description Respiratory Test Reader Acucy™ CLIA Waived Respiratory Test Reader LumiraDx™ TOP Program Respiratory Test Reader LumiraDx™ CLIA Waived Respiratory Test Reader Cue™ CLIA Waived Respiratory Test Reader Binaxnow® CLIA Waived
Manufacturer # 1039L016-US01-SB003L001000330001C0201LFR124
Brand Acucy™LumiraDx™ TOP ProgramLumiraDx™Cue™BinaxNOW®
Manufacturer Sekisui DiagnosticsLumiraDx IncLumiraDx IncCue Health IncAbbott Rapid Dx North America LLC
Invoice ACUCY SYSTEM, FLOW READER W/ACCESSORIES FULL PURCH OPT D/SPACK, STARTER LUMIRADX TOP PROGRAM W/SWABS CNTRL INSTR (D/S)INSTRUMENT, LUMIRADX D/SREADER, COVID-19 RAPID F/C2020&C2021 TEST KITCOMPLETE KIT, READER/MONITOR ALERE NOW RAPID OBJECTIVE D/S
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Comparison

Analyzer Type BenchtopBenchtopBenchtopHandheldBenchtop
CLIA Classification CLIA Waived for Swab SamplesCLIA WaivedCLIA Waived
CLIA Classified CLIA WaivedCLIA WaivedCLIA WaivedCLIA Waived
Contents 1 Acucy Reader, Acucy Printer, Acucy Calibration Device, (2) AC/DC Power Converters, Exclusive USB Memory Drive, Acucy System Manual, Printer Roll, Master Password CardCue Reader, Power Adaptor, Power CordAlere™ Reader, Barcode Scanner, Alere Binaxnow® Tray Pack, Calibration Check Card Pack, Alere™ USB Drive
Country of Origin JapanUnknownUnknownUnknownJapan
Dimensions 120 X 145 X 235 mm (Reader)73 X 97 X 210 mm73 X 97 X 210 mm1-1/2 X 2-7/8 X 2-7/8 Inch125 X 160 X 195 mm
For Use With For use with LumiraDx Test Strips / LumiraDx ConnectFor use with Cue Cartridges and Cue Health App on a Mobile Smart DeviceFor Alere™ Reader
Number of Tests 22 Tests
Power Source 100 to 240 V, 50/60 Hz100 to 240V, 50/60Hz100 to 240V, 50/60HzRechargeable Battery100 to 240 VAC, 50/60 Hz
Product Dating McKesson Acceptable Dating: we will ship >= 90 days
Purchase Program Type Standard Purchase AgreementPromotional BundleStandard Purchase AgreementStandard Purchase AgreementStandard Purchase Agreement
Readout Type USB Data Transfer / PrintoutTouchscreen DisplayTouchscreen DisplayTouch Screen, Printout
Sample Type Nasal Swab / Nasopharyngeal SwabCapillary Blood Sample / Nasal Swab SampleCapillary Blood Sample / Nasal Swab SampleNasal Swab SampleNasal Swab / Nasopharyngeal Swab
Test Name Influenza A + B TestSARS-CoV-2 Ag, SARS-CoV-2 Ab, D-Dimer, Prothrombin Time (INR), SurveillanceCOVID-19Influenza A + B Test
Time to Results 15 Minute Results20 Minute Results15 Minute Results
UNSPSC Code 4111580041115808411158194111580041115808
User Interface LCD Touch ScreenHigh Contrast Touch Screen / Barcode ScannerHigh Contrast Touch Screen / Barcode Scanner4-1/3 Inch Touch Screen
Weight 1.7 kg (Reader)2.42 lbs.2.42 lbs.5.3 oz.3.3 lbs
Application Respiratory Test ReaderRespiratory Test ReaderRespiratory Test ReaderRespiratory Test ReaderRespiratory Test Reader
Features and Benefits
  • Innovative Composite Comparator with molecular and culture
  • Read Now or Walk Away mode
  • Results within 15 minutes
  • The Acucy Reader is an optoelectronic instrument that uses a reflectance-based measurement method to evaluate the line signal intensities on the test strip, and a specific algorithm to determine the presence or absence of any target analyte(s)
  • LumiraDx TOP Program Starter Pack (7 Kits), Includes Instrument, Kits, Controls, Swabs
  • The LumiraDx Platform is an innovative, next generation point of care system that combines a small, portable instrument, advanced low cost test strip and seamless digital connectivity
  • Enzyme and immunoassay on a single platform
  • Its proprietary technology enables it to deliver exceptional point of care clinical performance, while being simple and easy to use
  • Performance referenced to laboratory test
  • Portable instrument, seamless connectivit
  • One simple, intuitive test workfow
  • Fast results in minutes
  • All common clinical samples
  • Small sample size including capillary blood
  • Ability to perform Quality Control Tests using LumiraDx Quality Control to meet regulatory compliance requirements
  • 2 x USB ports, RFID reader 13.56 MHz, 0 dBi (EIRP), Bluetooth low-energy 2.4 GHz ISM band, 2400 MHz to 2483.5 MHz, 0.5 dBm (ERP)
  • Lithium ion polymer 7.4 V 5000 mAh battery
  • High contrast touchscreen with a wide viewing angle
  • Uses small sample volumes and multiple convenient sample types, including nasal swab and capillary blood
  • Pipeline of 30+ assays, initially focused on some of the most common conditions being diagnosed or managed with POC testing
  • The LumiraDx SARS-CoV-2 Ag Test has been authorized by FDA under an EUA only for the detection of SARS-CoV-2 nucleocapsid protein
  • The LumiraDx SARS-CoV-2 Ab Test has been authorized by FDA under an EUA only for detecting the presence of total antibodies to SARS-CoV-2
  • Cue Reader is a durable, intuitive automated processor of test results and is used with Cue tests and the Cue Health App - designed to work with Cue's COVID-19 tests as well as future tests
  • The Cue Reader runs single-use cartridges and communicates the result of the test digitally via Bluetooth® to the Cue Health App
  • The Cue Cartridge Reader features 5 LED indicator lights located on the top of the Cue Cartridge Reader
  • Once the Cue Wand with the nasal sample is inserted into the pre-heated Cue Test Cartridge, the Cue Reader will process the test and communicate the result directly to the Cue Health App on your mobile device via Bluetooth®
  • The lights provide quick feedback on the status of the Cue Cartridge Reader together with the Cue Health App
  • Cue is the first compact, portable molecular self-testing system authorized by the FDA for use at home or on the go, without a prescription
  • Cue COVID-19 tests sold separately
  • Alere BinaxNOW® Influenza A & B Card 2 is an in vitro immunochromatographic assay for the qualitative detection of influenza A and B nucleoprotein antigens in nasopharyngeal (NP) swab and nasal swab samples
  • Alere BinaxNOW® Influenza A & B Card 2 must be read by the Alere™ Reader
  • The first rapid antigen influenza test to achieve 510(k) clearance as a Class II assay under the new FDA Reclassification performance requirements