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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

Fujirebio Diagnostics

LUMIPULSE G1200

Company

Fujirebio Diagnostics

Name of instrument

LUMIPULSE G1200

Contact

Christopher Joynes  

Email

 joynesc@fdi.com

City, State

Malvern, PA

Phone

844-544-3787   

Website

http://www.fujirebio.com

Type of instrument

immunoassay

List price/First year sold in U.S.

$175,000/2016

Targeted hospital bed size/Targeted test volume

> 50/daily: 1,000; monthly: 20,000; annual: 240,000

Company manufactures instrument

no (manufactured by Otsuka)

Other models in this family of analyzers

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

>60/~1,500 (Japan, Germany, France, Italy, Belgium)

Dimensions (H × W × D)/Instrument footprint

57.6 × 47.2 × 31.5 in./35 sq. ft.

Weight empty/Weight fully loaded

727 lbs./794 lbs.

No. of different measured assays onboard simultaneously

36 (24 can be run and calibrated at one time)

No. of user-definable (open chemistry) channels

Test throughput per hour/Assay run time

120 (120 tests in throughput)/30 min.

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

chemiluminescence

Separation methodologies

magnetic particle

Stat time until completion of a ß-hCG test

30 min.

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°–10°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/yes

Walkaway capability/Walkaway duration

yes/55 min. or 100 specimens or 155 tests

Design of sample-handling system

rack

Uses washable cuvettes/Uses disposable cuvettes

no/no

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

10–140 µL

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

150 µL/110 µL/100 µL

Dedicated pediatric sample cup

no

Primary tube sampling

yes

Accommodates most standard tube sizes/Accepts nonstandard tube sizes

yes/yes

Pierces caps on primary tubes

no

Protects against probe collision

no

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

no (calibrants are not stored onboard)/yes (recommended avg. frequency: 30 days)

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

—/—/—/—/30 days

Automatic programmable start/Automatic programmable shutdown

yes (5 min. warm-up time)/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 direct to drain

Sample barcode-reading capability/Autodiscrimination

yes (Interleaved 2 of 5, Codabar, Code 39, Code 128, NW7, Standard 2 of 5)/no

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

no

UPS backup power supply

yes

Data-management capability/LIS or EHR systems interfaced

onboard/SCC Soft Computer

LIS interface provided/Bidirectional interface capability

yes (included in instrument price)/yes (broadcast download and host query)

Modem servicing provided/Service engineer on-site response time

no/24 hrs.

Mean time between failures

>300 days (displays error codes for troubleshooting)

Average scheduled maintenance time by lab personnel

daily: 15 min.; weekly: 30 min.; monthly: 45 min.

Maintenance records kept onboard for user/vendor

no/no

Maintenance training demonstration module onboard

yes (2 training slots per module)

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

yes/8 hrs. (at customer site)

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

yes (at customer site)/yes ($2,500 [post-instrument install])

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

yes (1 year)/$14,950

Distinguishing features (supplied by company)

unitized test cartridge (14 tests/cartridge) reduces reagent waste and eliminates cross contamination; continuous access loading and unloading of samples, reagents, and consumables without operational interruption; 30-min. time to result for all assays

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