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Tuesday, July 21, 2026, 11:00-11:30 AM CT
- Explain how transparency and manufacturer partnerships improve quality, consistency, and decision-making confidence in specimen management.
- Evaluate blood collection tubes beyond cost and commodity assumptions, incorporating clinical impact and risk into decision-making.
- Assess the potential risk points when using a blood collection device that has not been cleared for a specific purpose.
Roundtable presenters Nick Fingland, PhD, PMP, Senior Director, R&D Operations and Science, BD, and Chris Farnsworth, PhD, D(ABCC), Section Head of Clinical Chemistry, Professor of Pathology and Immunology, Washington University School of Medicine.
Moderated by: Bob McGonnagle, Publisher, CAP TODAY
Wednesday, July 29, 2026, 1:00-2:00 PM ET
Learn about digital pathology technology that is future-ready, yet practical for today’s
laboratory needs.
Webinar presenters Scott Hammond, Senior Systems Consultant, Digital Pathology Division, Wexner Medical Center, Department of Pathology, and Ursula Hofer, Imaging Technologist, Pathology Digital Imaging Lab, Wexner Medical Center, Department of Pathology, and Sandra Banky, PA(ASCP), Director of Operations, Wexner Medical Center, Department of Pathology.
Moderated by: Bob McGonnagle, Publisher, CAP TODAY
Interactive Product Guides
Product Spotlight
Beckman Coulter
DxU Iris Workcell: DxU 850 Iris, DxU 840 Iris
| Company | Beckman Coulter |
|---|---|
| Name of urinalysis instrument | DxU Iris Workcell: DxU 850 Iris, DxU 840 Iris |
| Contact | Kanochia Johnson |
| City, State | Brea, CA |
| Website | |
| Type of instrument | urine chemistry and microscopy/sediment combined |
| Instrument list price | — |
| First year instrument sold in the U.S. | 2021 (also sold by McKesson, Henry Schein in U.S.) |
| Approximate No. of units in clinical use in the U.S./outside the U.S. | >800/>120 (worldwide) |
| Foreign countries where company markets instrument | worldwide |
| Country where instrument is designed/manufactured | U.S./U.S. and Japan |
| Human languages (other than English) supported | French, German, Spanish, Portuguese, Italian, many more |
| Intended urine sample volume per day | 50–600+ |
| Dimensions (H×W×D) | 23 × 21 × 60 in. |
| Weight fully loaded with reagents/without reagents | 238 lbs./214 lbs. |
| Power requirements | 100–240 VAC (50–60 Hz) |
| Mean time between failure of instrument | 305 days |
| Events that cause instrument to lock or stop analysis | QC failure, short sample, barcode/sample ID misread, result error, sampling error, consumables replacement/expiration |
| • Urine chemistry tests available on instrument in the U.S. | bilirubin (0–>10 mg/dL), hemoglobin (0–>1 mg/dL), glucose (0–>1,000 mg/dL), ketone (0–>150 mg/dL), leukocyte esterase (0–500 leukocytes/µL), nitrite (–, 1+, 2+), pH (5–9), protein (0–>600 mg/dL), specific gravity (1.0–1.5), urobilinogen (0–≥12 mg/dL) |
| • Color compensation pad included/Flagging thresholds customizable | yes/no |
| • Test strip configuration | loosely packed in bottles |
| • Calibration required after each test strip lot No. change | no |
| • Frequency of customer-performed calibration/Form of calibration | monthly/liquid |
| • How results are displayed for urine chemistry | semiquantitative |
| • Specific gravity correction for protein/glucose | yes/yes |
| • Microscopy/sediment technology | digital flow morphology using auto particle-recognition software |
| • Microscopy/sediment analysis parameters | qualitative and quantitative: pathological casts, crystals, yeast-like cells, mucus, sperm, RBCs, WBCs, epithelial cells, bacteria, hyaline casts, WBC clumps |
| • Flagging thresholds customizable | yes |
| • Instrument eliminates amorphous crystal interference before sample analysis | no |
| • How results are displayed for microscopy/sediment | numeric values |
| • Reporting format customizable | yes |
| • No. of results that can be held in internal memory | 10,000 sample results/200 control results |
| Reagent shelf life/storage temp. for unopened containers of calibrator | both vary based on reagent type |
| Reagent shelf life/storage temp. for opened containers of calibrator | both vary based on reagent type |
| Reagent shelf life/storage temp. for unopened containers of control reagent | both vary based on reagent type |
| Reagent shelf life/storage temp. for opened containers of control reagent | both vary based on reagent type |
| Reagent barcode-reading capability | yes, for some tests (can read Code 39, Code 128, more) |
| How often quality control samples are run | daily |
| Sample throughput per hour/Time to first result for chemistry | 225/1 min. |
| Sample throughput per hour/Time to first result for microscopy/sediment | DxU 840: 70/<2 min.; DxU 850: 101/<2 min. |
| Analyzer has stat mode | no (min. sample volume for sampler or track mode, 2 mL for chemistry and 3 mL for microscopy/sediment) |
| FDA approved for body fluid analysis | yes (for CSF, pleural, peritoneal, synovial, more) |
| Sample dilutions required for urinalysis/body fluid analysis | no/yes (lyse reagent required) |
| Minimum width of sample tube/Minimum length of sample tube | 16 mm/100 mm |
| Conditions or substances that prevent a sample from being run | grossly visible turbidity |
| Means of sample ID entry | barcode scan, manual entry |
| Built-in liquid-level sensing for samples | yes |
| Information that can be barcode scanned on instrument | specimen identifier, reagent lot No., reagent expiration, dilution barcodes |
| Compatible with laboratory automation systems | no |
| How LOINC codes for results are made available | website |
| Software includes reflex testing/cross-check functionality | yes/no |
| Instrument automatically generates consolidated report* | yes |
| Instrument archives patient data | yes (patient results) |
| Instrument connections to transfer information | directly to LIS |
| Interface standards or formats supported | ASTM 1381, ASTM 1238-95, Iris-defined XML |
| Bidirectional interface | yes, to other companies’ LISs |
| Test results can be transmitted to LIS as soon as tests completed | yes |
| Connection to LIS/EHR to upload patient and QC results | LIS: direct serial/EHR: — |
| Information included in transmission to data-management system | device unique identifier, operator ID, patient ID, specimen ID, result, QC identifier |
| Training included with instrument purchase | yes (1 day at customer site, 3 days of e-learning; follow-up training available for an extra charge) |
| Approximate scheduled maintenance time required | — (maintenance records kept onboard instrument) |
| Onboard diagnostics for troubleshooting | yes |
| Provide list of client sites to potential customers on request | yes (complete list with no restrictions regarding its use) |
| Clients restricted from sharing their experience with company or software | no |
| Distinguishing instrument features (supplied by company) | auto-classifies 12 urine particles based on size, shape, contrast, texture to provide digital images for all samples; iQ Body Fluids Module analyzes RBC count and nucleated cell count in cerebrospinal, synovial, and serous fluids |
| *chemistry and microscopy results in one report; Note: a dash in lieu of an answer means company did not answer; question or question is not applicable | †formerly iQ Workcell; all answers apply to DxU 850 Iris and 840 Iris systems unless otherwise indicated |