Atellica CI Spec Sheet
Atellica CI Spec Sheet
Atellica CI Spec Sheet
Atellica CI Analyzer
The Atellica® CI* Analyzer addresses big challenges—
all in a compact 1.9 m2 footprint
siemens-healthineers.com/atellica-ci-analyzer
Sample Handling
Validated Sample Types Serum, plasma, amniotic fluid, urine, whole blood (assay-specific), CSF, and other
Sample Integrity Control Liquid-level sensing, clot/clog detection, bubble detection, short-sample detection; hemolysis,
icterus, and lipemia
Auto-repeat Automatic repeat testing from the original and diluted samples
Sample Dilution Assay-dependent; can be auto-diluted and repeated when results extend linearity
Auto-reflex Testing Configurable; additional tests based on results of first test or test mix
Sample Carryover Prevention Chemistry uses precision wash system.
Immunoassay uses disposable sample tips to eliminate carryover.
Sample Volume per Test 2–100 μL of sample (varies by assay)
Reaction Area
Reaction Cuvettes CH dilution cuvettes (64 reusable cuvettes: four segments with 16 cuvettes each)
CH reaction ring segments (clinical chemistry = 130 reusable cuvettes, 10 segments, 13 cuvettes)
IM incubation ring holds 56 cuvettes.
Reaction Temperature CH: 37°C ±0.3°C, IM: 37°C ±0.4°C
Chemistry Reaction Detection Reaction area: photometer, LED light source with 11 fixed wavelengths (340, 410, 451, 478, 505,
545, 571, 596, 658, 694, 805 nm). Linearity: 0–3.0 AU. Resolution: 0.0001 AU.
Chemistry Assay Calculations Endpoint (EPA), rate reaction (RRA), 2-point rate (2PA), sample blank correction
Immunoassay Reaction Detection Photomultiplier tube
Immunoassay Reaction Formats Sandwich, competitive, and antibody-capture/antigen-bridge formats
Assay Time Chemistry and immunoassay: 1–54 minutes, assay-dependent
Assay Technology CH: Integrated Multisensor Technology (IMT, electrolytes), photometric, and turbidimetric
IM: chemiluminescence testing methodology using advanced acridinium ester technology
Reagent Handling
Reagent Compartments CH: one tray (70 positions), refrigerated, temperature-controlled compartment 4–12°C
IM: 20 primary, 20 ancillary reagent positions with refrigeration and humidity control, continuous
and automatic mixing to maintain particle suspension, temperature-controlled compartments 4–10°C
Reagent Packs CH: 50 mL dual-well reagent containers (2 x 25 mL each); 95–2100 tests per pack
IM: ReadyPack® cartridge: 50–200 tests per pack
Reagent Integrity Control Reagent pack barcode identification: automatic pack/well tracking, notification of inventory, calibration
and control validity, onboard stability, low and expired reagents, detection of reagent bubbles
Onboard Stability CH: up to 6 months (assay-dependent)
IM: up to 3 months (assay-dependent)
Dispensing System CH: one probe with liquid-level sensing and crash detection
IM: one probe with liquid-level sensing and crash detection
Barcode-labeled Packs Yes
Average Reagent Volume 10–100 μL per test, assay-dependent
Open Channels CH only: available. Configurable to assay specifications with ability to copy Atellica CH assays
and configure per laboratory needs.
Integrated Multisensor Technology (IMT) for Na+, K+, Cl− (CH only)
Assay Time 18 seconds
Sample Volume 25 μL produces three results
Sample Dilution Automatic 1:10; automatic monitoring for bias with every patient result
Calibration Automatic calibration
Priming Automatic priming cycle
A-LYTE™ Integrated Multisensor Up to 5000 samples or 14 days
Technology Cartridge Use Life
Calibration/QC
Auto-calibration Automatic calibration orders generated by test definition for
CH and IM assays.
Calibration Review Graphical display of calibration curves for a minimum
of 20 different reagent lots and 20 reagent packs for each assay
with autovalidation.
Auto-QC Automatic QC orders generated by test definition for CH
and IM assays. Quality control testing can be automatically
ordered by day, time, panel, test count, control material, Atellica Portfolio of
Laboratory Products
and with calibration orders.
Quality Control Review Advanced QC package with graphical display of QC in real time,
including patient moving averages, Levey-Jennings plots,
Westgard rules, RiliBÄK rules; up to 125,000 control results can
be stored; autovalidation, archivable to removable media. Engineered by
QC/Calibration Material QC and calibration materials are tracked in the software by test
definition and sequence number. Includes onboard stability and
Siemens Healthineers
interval expiration. to deliver control and
Laboratory Evaluations Patent-pending assay evaluation suite. Provides onboard
support for precision testing, automatic and manual measuring
simplicity so you can
interval verification studies, QC parallel and reagent lot-to-lot drive better outcomes.
testing.
Maintenance
Address staff shortages and
Daily Hands-on: <5 minutes; automated: ≤30–45 minutes
Weekly Hands-on: <4 minutes; automated: up to 75 minutes
burnout, make patient care
Monthly Hands-on: <5 minutes more predictable, and
As Needed Refer to online help for additional periodic maintenance. empower the lab to be more
Logs Operator, Maintenance, LIS, and Audit Trail logs monitor agile in today’s changing
activities via the software. Monthly approvals, stored on the
system, printable, exportable, and formatted for inspections.
world—all critical aspects in
today's evolving healthcare
General Specifications landscape. That’s the promise
Power Requirements Voltage: 200–240 VAC, current: 24 A, frequency: 50/60 Hz
5.0 m power cord with IEC 60309 (6H) 30A/250V 2P+E plug
of our Atellica® portfolio of
(OUS) or NEMA L6-30 plug (U.S.) laboratory products.
IEC 60309 (6H) 30A/250V 2P+E receptacle required (must be
supplied by the facility).
Power Consumption 2.2 kW
Water Input Requirements Incoming pressure 5–30 psi at 10–30°C
Water Quality Special reagent water (SRW) required:
Requirements • Resistivity: ≥10 MΩ/cm
• Bacteria: ≤50 CFU/mL
• Total organic carbon: ≤500 ppb
A 0.22 micron filter is required at the output stage of the
laboratory. An additional 0.22 micron filter is required before
the input to the water supply.
Maximum Water Consumption Up to 25 liters of water per hour at maximum instrument capacity.
Drain Requirements 76.2 mm (3 in.) drain is recommended to handle
minimum of 100 L/hour (1.7 L/min).
Dimensions† (H) 1600 mm, (W) 2034 mm, (D) 934 mm = <1.9 m2
Weight 760 kg (1675.5 lb)
Compliance Complies with international environmental, health,
and safety standards, including CE and RoHS.
Noise Emission Complies with NC-43 noise control specification. Average
sound pressure of <65 dBA 1 m from analyzer.
Processing Heat Output 7500 BTU/hr
Ambient Temperature 18–30°C (64–86°F)
Ambient Humidity 20–80% noncondensing
Altitude Up to 2000 meters
Floor Load-bearing Requirement 400 kg/m2, seismic anchoring available
Overvoltage Classification Category II
Pollution Classification Degree 2
Removable Media USB
Published by Siemens Healthcare Diagnostics Inc. · CLS-23-2921-76 · HOOD05162003368734 · 08-2023 · © Siemens Healthcare Diagnostics Inc., 2023