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Tuesday, July 21, 2026, 11:00-11:30 AM CT

Learning Objectives:
  • 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

Subspecialties

Interactive Product Guides

Product Spotlight

Bio-Rad Laboratories Clinical Diagnostics Group

BioPlex 2200 System

Company

Bio-Rad Laboratories Clinical Diagnostics Group

Name of instrument

BioPlex 2200 System

Contact

Maria Crisostomo   

Email

maria_crisostomo@bio-rad.com

City, State

Hercules, CA

Phone

800-224-6723   

Website

http://www.bio-rad.com

Type of instrument

immunoassay

List price/First year sold in U.S.

—/2006

Targeted hospital bed size/Targeted test volume

—/daily: ~800 samples

Company manufactures instrument

yes

Other models in this family of analyzers

No. of units in clinical use in U.S./Outside U.S. (countries)

—/— (Australia, Canada, China, Europe, Hong Kong, Israel, Japan, Korea, New Zealand, Russia, Saudi Arabia)

Dimensions (H × W × D)/Instrument footprint

53 × 72 × 34 in./12.9 sq. ft.

Weight empty/Weight fully loaded

1,032 lbs./—

No. of different measured assays onboard simultaneously

51 (51 can be run and calibrated at one time)

No. of user-definable (open chemistry) channels

Test throughput per hour/Assay run time

up to 2,200 (up to 22 tests in throughput)/avg. 45 min. (assay dependent)

No. of direct ion-selective electrode channels

Detection methods

Stat time until completion/specimen throughput for Ion-selective electrode

Stat time until completion/specimen throughput for Ion-selective electrode basic metabolic panel

Stat time until completion/specimen throughput for Ion-selective electrode complete metabolic panel

Typical time delay from ordering stat test until aspiration of sample

Fully automated microplate immunoassay system

no

Methodologies supported

multiplex flow (cytometric)

Separation methodologies

magnetic particle

Stat time until completion of a ß-hCG test

Stat time until completion of a cTn test

• Typical time delay from test order to aspiration of sample

Reagents refrigerated onboard/Reagents ready to use

yes (2°–8°C)/yes

Reagent lot tracking/Reagent inventory

yes/yes

Reagent form/Reagents barcoded

liquid chemistry (closed reagent system)/yes

Separate reagent pack for each specimen/for each test run

no/no

Walkaway capability/Walkaway duration

yes/480 min. or 800 specimens or 9,600 tests

Design of sample-handling system

rack

Uses washable cuvettes/Uses disposable cuvettes

no/—

Min.–max. sample volume that can be aspirated at one time 

3–150 µL

Min. reaction volume/Min. specimen volume/Min. dead volume

3 µL/350 µL (tube size dependent)/250 µL

Dedicated pediatric sample cup

no

Primary tube sampling

yes

Accommodates most standard tube sizes/Accepts nonstandard tube sizes

yes/no

Pierces caps on primary tubes

no

Protects against probe collision

yes

Detects clots/liquid level/short sample

yes/yes/yes

Detection or quantitation for hemolysis, icterus, lipemia, clots

detection for clots; hemolysis, icterus, lipemia not available

Dilutes patient samples onboard/Susceptibility to carryover

yes (can be programmed to perform dilutions prior to analysis)/<1 part per million

Automatic rerun capability

no

Sample volume can be diluted to rerun out-of-linear-range high results

yes

Sample volume can be concentrated to rerun out-of-linear-range low results

no

Autocalibration/Multipoint calibration supported

yes (calibrants are not stored onboard)/yes (recommended avg. frequency: 30 days [assay dependent])

Typical calibration frequency for ISE/therapeutic drugs/drugs of abuse/general chemistries/immunoassays

—/—/—/—/30 days (assay dependent)

Automatic programmable start/Automatic programmable shutdown

yes/—

Onboard real-time QC/Onboard software capability to review QC

yes/yes

Supports multiple QC lot numbers per analyte

yes

Waste management

manually by user or automated collection onboard instrument or direct to drain

Sample barcode-reading capability/Autodiscrimination

yes (Interleaved 2 of 5, Codabar, Code 39, Code 128)/yes

Lab can control analyzer from remote computer

no

Instrument can diagnose its own malfunctions

yes (operator intervention required to order parts)

System malfunctions can be diagnosed via remote monitoring

yes

UPS backup power supply

yes

Data-management capability/LIS or EHR systems interfaced

onboard/Antrim, CCA, Oracle Health, CGM Schuylab, SCC Soft Computer, Meditech, Clinisys, more

LIS interface provided/Bidirectional interface capability

no/yes (broadcast download and host query)

Modem servicing provided/Service engineer on-site response time

yes/< 24 hrs.

Mean time between failures

— (displays error codes for troubleshooting)

Average scheduled maintenance time by lab personnel

daily: 5 min.; weekly: 30 min.; monthly: ~60 min.

Maintenance records kept onboard for user/vendor

yes/yes (both include audit trail of who replaced parts)

Maintenance training demonstration module onboard

no

Training included with purchase/Avg. time for basic user training

yes (2 training slots)/5 days (at vendor site)

Advanced operator training/Extra charge for follow-up or advanced training

no/yes

Warranty provided/Cost of annual service contract (24 h/7 d)

yes (1 year)/—

Distinguishing features (supplied by company)

full random-access automation with innovative multiplex chemistry; internal QC beads for monitoring test performance; 51 assays: 26 autoimmune, 24 infectious disease, vitamin D; compatible track line connectivity option; CylancePROTECT Antivirus program provides digital protection against malware

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