official distributor for Bulgaria

ADVIA Centaur XPT Immunoassay System

An advanced automated immunoassay analyzer designed for continuous operation.

The ADVIA Centaur® XPT Immunoassay System is engineered for simplified, continuous operation and timely, trusted results.

  • Responds to peak testing needs with a throughput of up to 240 tests per hour and no-pause loading of reagents, consumables, and samples.
  • Supports comprehensive diagnoses with a menu of over 70 assays.
  • Continually expands testing with advanced acridinium ester technology—evolving chemiluminescence that provides the flexibility to meet changing clinical needs.

Cutting-edge AE Immunoassay Technology

  • Meet evolving clinical needs with advanced acridinium ester technology, which provides flexibility and sensitivity for new and innovative assays.
  • Manage comprehensive disease-state testing with a menu of more than 70 assays.
  • Simplify inventory management and reduce cost with the same highly stable, ready-to-use reagents used on all ADVIA Centaur analyzers.

Simplified, Continuous Operation

  • Load and unload all samples, reagents, and supplies without pausing the system.
  • Simplify operation and training with an intuitive, icon-driven user interface.
  • Reduce hands-on time with low daily maintenance and no monthly cleaning or daily startup procedures.
  • Implement new assays immediately with one easy scan of a test definition bar code.

Consistent, Predictable Turnaround Time and Accuracy

Deliver up to 240 tests per hour for fast turnaround, even during peak workload times.

  • React fast with a STAT port that allows priority sampling at any time.
  • Improve result integrity with disposable probe tips that eliminate sample-to-sample carryover.
  • Conduct automatic repeat and confirmatory testing of reactive hepatitis B surface antigen samples using Siemens Healthineers unique SMART algorithm software.

Seamless Connectivity

See how Labor Blackholm MVZ increased testing volume by 34% with 30% fewer analyzers

  • Adapt and grow as workloads demand by connecting directly to Aptio® Automation and VersaCell® X3 Solution.
  • Streamline operations with diagnostics IT, including CentraLink® Data Management System, Atellica® Process Manager and Siemens Remote Service (SRS).
  • Sample directly from the track using point-in-space technology.
  • Drive rapid turnaround time with a dedicated STAT port that can also front-load priority samples when connected to automation.
Anemia
Active B12
EPO
Ferritin
Folate
RBC Folate
Vitamin B12

Anti-CCP IgG

Intact PTH
Vitamin D Total
BNP
CKMB
High-Sensitivity Troponin I
Myoglobin
NT-proBNP
C-Peptide
Insulin
Growth Hormone hGH
IGF-1
IFBP-3

Anti-HBe2
Anti-HBs 2
HAV IgM
HAV Total
HBc IgM
HBc Total 2
HBeAg
HBsAg Confirmatory
HBsAg II
HBsAg II Quant
HCV

HIV Ag/Ab Combo (CHIV)

Cyclosporine
Everolimus
Sirolimus
Tacrolimus
IgE Total
IL-2
IL-6
LBP
TNFα
Enhanced Liver Fibrosis (ELF™) Test
HA (ELF™ Marker)
PIIINP (ELF™ Marker)
TIMP-1 (ELF™ Marker)
Cortisol
Homocysteine
β-Amyloid 1-42(AB42)
sNfL
Total Tau (TTAU)
AFP
BR 27.29
CA 125II
CA 15-3
CA 19-9
Calcitonin
CEA
Complexed PSA
CYFRA 21-1
Free PSA
Neuron Specific Enolase (NSE)
PSA
Serum HER-2/neu
Squamous Cell Carcinoma Antigen (SCC)
AFP
Androstenedione
Anti-Müllerian Hormone
DHEA-SO4
Enhanced Estradiol
Free Beta HCG
FSH
hCG
LH
PAPP-A
PlGF
Progesterone
Prolactin
sFLT-1
SHBG
Testosterone II
Procalcitonin (PCT)
EBV-EBNA IgG
EBV-VCA IgG
EBV-VCA IgM
SARS-CoV-2 Ag (CoVAg)
SARS-CoV-2 IgG (sCOVG)
SARS-CoV-2 Total (COV2T)
Syphilis
Zika Test
Digoxin
aTgII
Anti-TPO
Free T3
Free T4
Total T3
Total T4
TSH3-Ultra
TSH
T Uptake
CMV IgG
CMV IgM
Herpes-1 IgG
Herpes-2 IgG
Rubella IgG II
Rubella IgM
Toxoplasma IgG
Toxoplasma IgM

Product specifications

System description

Random-access immunoassay system with direct chemiluminescence testing methodology using
advanced acridinium ester technology

Test throughput

Up to 240 tests per hour in batch or random-access mode

Walkaway time

2 hours (at maximum throughput)

Sample handling

Validated sample types

Serum, plasma, urine (varies by assay)

Sample integrity control

Pressure-based level sensing, short-sample detection and flagging, clot detection and flagging,
foamy sample detection, ambient temperature detection and flagging

Auto-repeat

User-defined automatic repeat testing from original sample

Sample dilution

Can be auto-diluted, up to 1:2500 (varies by assay)

Auto-reflex testing

User-defined automatic reflex testing

Sample carryover prevention

Disposable pipette tips eliminate sample carryover

Sample volume per test

10–200 μL of sample (varies by assay)

Sample bar code

Code 39; Codabar; Code 128; Interleaved 2 of 5 (any of the symbologies may be active at one time)

Sample tubes

1 mL, 2 mL sample cups; 3 mL, 5 mL, 7 mL, 10 mL tubes; microtainer tubes

Sample capacity

180 samples, continuous loading, in universal 5-position sample racks

Pipette tips

ADVIA Centaur type; 840 onboard, automatic tracking and notification

STAT handling

Dedicated STAT position accepts samples at any time

Reaction area

Reaction cuvettes

Onboard capacity of 1000 ADVIA Centaur cuvettes

Reaction bath

Air bath, 37°C (98.6°F)

Assay times

18 minutes; results every 15 seconds thereafter, assay-dependent

Assay technology

Direct chemiluminescence testing methodology using advanced acridinium ester technology

Reagent handling

Assays onboard

30

Primary ancillaries

30-position cooled storage with refrigeration at 4–10°C (39.2–50°F)

Reagent ancillaries

25-position cooled storage with refrigeration at 4–8°C (39.2–46.4°F)

Reagent packs

ReadyPack® cartridge

Reagent integrity control

Reagent pack bar-code identification; automatic tracking and notification of inventory,
calibration validity, reagent onboard residency, reagent expired/low flags

Onboard stability

Up to 28 days, assay-dependent

Reagent inventory management

Automatic tracking and notification of remaining tests, onboard residency, calibration,
and reagent expired/low flags

Reagent preparation

None required

Bar code-labeled packs

Yes

Calibration/QC

Auto-calibration/QC

Available automatic QC ordering by test, control, date, and time

Calibration identification

Bar-coded labels containing lot-specific data; human- and system-readable through handheld
bar-code scanner

Calibration status

Tracking and notification of calibration status, including advance notice of pending expiration;
user-defined processes for response of calibration expiration

QC package

Advanced QC package for long-term monitoring, including L-J plots and Westgard rules

QC levels

0–9 control levels per assay

QC definitions

User-defined

QC result storage

1,000,000 control, patient, and event results can be stored in the database

Maintenance

Daily

Automated: 65 minutes; hands-on: 0 minutes

Weekly

Hands-on: 30 minutes

Maintenance logs

Automated onboard scheduling, notification, and reporting

User interface/data management

Monitor

22-inch diagonal LCD touchscreen

Operating system

MICROSOFT WINDOWS 10

Remote access and service

Smart Remote Services

General specifications

Power requirements

200–240 V, 50/60 Hz; 1.2 kW maximum

Water input requirements

Type 1 reagent water guidelines as specified by the Clinical Laboratory and Standards Institute (CLSI);
at minimum, water quality should meet CLSI Type II guidelines

Water quality requirements

Bacterial content: >50 ppb total organic compounds

Maximum resistivity: 1 megohm/cm

Maximum water consumption

2.5 liters (0.6 gallons) per hour

Drain requirements

Minimum of 2.5 liters (0.6 gallons) per hour

Dimensions

133 (h) x 196 (w) x 104 (d) cm

52 (h) x 77 (w) x 41 (d) inches

(excluding monitor and accessories)

Weight

585 kg (1289 lb) (including monitor and accessories)

Compliance

Complies with international environmental, health, and safety standards, including CE and RoHS

Floor load-bearing requirement

412 kg/m2 (84 lb/ft2)

Noise emission

Up to 65 dB (with normal use)

Processing heat output

5100 BTU/hour

Ambient temperature

18–30°C (64–86°F)

Ambient humidity

20–80% noncondensing

Overvoltage classification

Main supply voltage fluctuations must be within ±10% of the nominal voltage

Pollution classification

IEC 1010-1 Pollution Degree 2

Why Choose Us

We believe that success is achieved with professionalism, integrity and perfect teamwork, built on the high moral values of our employees.
Our policy is based on impeccable planning, control and execution, through which we achieve maximum satisfaction of our customers.

Professional
customer service

A wide range of laboratory analyzers

Trained and experienced specialists

Certificate
ISO 13485:2012