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ADVIA Centaur CP Immunoassay System
Why should a lab have to sacrifice speed and efficiency for quality?
The ADVIA Centaur® CP Immunoassay System is a mid-volume, high-throughput bench top system that enhances your in-house test capability. With its broad menu and short Turn Around Times (TAT), you can do more — without compromising efficiency, productivity, or quality. And it features the superior sensitivity and specificity you expect of Chemiluminescent with Advanced Acridinium Ester Technology.
The ADVIA Centaur® CP Immunoassay System is a surprisingly powerful and fast mid-sized immunoassay system. This consolidated platform with its enhanced menu capacity improves workflow and decreases costs by eliminating the need for multiple systems.
Patient Care
The ADVIA Centaur CP Immunoassay system allows your lab to provide excellent patient care by bringing a wide range of immunoassays onto a single workstation, including infectious disease and Serum HER-2/neu.
- Comprehensive disease state testing menu
- Disposable pipette tips
- STAT testing and test prioritization
- TAT in as little as 15 minutes for most assays
- Sample and reagent bubble detection, and sample clot detection
- Constant visibility to time to result for each test
Increased Productivity
The ADVIA Centaur CP Immunoassay System raises the level of productivity and increases the efficiency of operations within your lab with these features:
- Up to 180 tests/hour throughput
- 400-test walkaway capacity
- Always accessible and visible sample compartment with a 84-sample capacity
- No-pause loading/unloading of samples and supplies
- 15 refrigerated reagents onboard with automatic mixing and a 10-reagent compartment for ancillaries such as diluents
- Programmable automatic dilutions, repeats and reflex testing
Ease of Use
The ADVIA Centaur CP Immunoassay System was designed with ease-of-use in mind. It allows for true continuous operation with the following features:
- Ready-to-use, barcoded reagents are automatically programmed into the software with no operator intervention
- Status bar warns operator when any supply or reagent is getting low before system processing is interrupted
- Automatic operator warnings included when calibration is close to expiring and when the need to perform maintenance is upcoming
- Simple maintenance requiring minimal hands-on time
- Intuitive touch screen operation, Windows®-based software
Quality
The ADVIA Centaur CP Immunoassay System uses the same time-proven Chemiluminescent Acridinium Ester technology as the rest of the ADVIA Centaur family, and the same features to maximize quality:
- Disposable pipette tips (zero carry over)
- Automated clot detection
- User-defined automatic reflex and repeat testing to insure accuracy
- Sample and reagent bubble detection to further ensure quality results
Flexible Solutions
The ADVIA Centaur CP Immunoassay System has the capacity to fit in several different scenarios. The ADVIA Centaur family of systems allow you to run tests from the satellite laboratory to the core laboratory utilizing the same technology and reporting the same quality results.
- Medium volume laboratories increase productivity through one platform
- Satellite and STAT facilities reduce time to result
- Specialty testing laboratories provide minimum TAT with a menu of specific assays
- Large primary and smaller secondary laboratories have the convenience and uniformity of results with the same reagents and consumables as the ADVIA Centaur XP Immunoassay System
With the ADVIA Centaur CP Immunoassay System, you can stay ahead of your growing test volume, maximize productivity, and meet the growing needs of your lab in less time and greater efficiency.
Anemia
EPO
Ferritin
Folate
RBC Folate
Vitamin B12
Autoimmune
Bone Metabolism
Cardiac
BNP
CKMB
High-Sensitivity Troponin I
Myoglobin
NT-proBNP
Diabetes
C-Peptide
Insulin
Growth
Growth Hormone hGH
IGF-1
IFBP-3
Hepatitis
Anti-HBe 2
Anti-HBs 2
HAV IgM
HAV Total
HBc IgM
HBc Total 2
HBeAg
HBsAg Confirmatory
HBsAgII
HCV
HIV
HIV Ag/Ab Combo (CHIV)
Immunosuppressant Drugs
Cyclosporine
Everolimus
Sirolimus
Tacrolimus
Inflammation
IgE Total
IL-2
IL-6
LBP
TNFα
Liver Fibrosis
Enhanced Liver Fibrosis (ELF™) Test
HA (ELF™ Marker)
PIIINP (ELF™ Marker)
TIMP-1 (ELF™ Marker)
Metabolic
Cortisol
Homocysteine
Neurology
β-Amyloid 1-42(AB42)
sNfL
Total Tau (TTAU)
Oncology
AFP
CA 125II
CA 15-3
CA 19-9
Calcitonin
CEA
Complexed PSA
CYFRA 21-1
Neuron Specific Enolase (NSE)
PSA
Serum HER-2/neu
Squamous Cell Carcinoma Antigen (SCC)
Reproductive Endocrinology
AFP
Androstenedione
Anti-Müllerian Hormone
DHEA-SO4
EnhancedEstradiol
Free Beta HCG
FSH
hCG
LH
PAPP-A
PIGF
Progesterone
Prolactin
sFLT-1
SHBG
Testosterone II
Sepsis
Procalcitonin (PCT)
Special ID
EBV-EBNA IgG
EBV-VCA IgG
EBV-VCA IgM
SARS-CoV-2 IgG (sCOVG)
SARS-CoV-2 Total (COV2T)
Syphilis
Zika test
Therapeutic Drug Monitoring
Digoxin
Thyroid
aTgII
Anti-TPO
Free T3
Free T4
Total T3
Total T4
TSH3-Ultra
TSH
T Uptake
ToRCH
CMV IgG
CMV IgM
Herpes-1 IgG
Herpes-2 IgG
Rubella IgG II
Rubella IgM
Toxoplasma IgG
Product specifications
System description
Random-access immunoassay system with direct chemiluminescence testing methodology using advanced acridinium ester technology
Test throughput
Up to 180 tests per hour in batch or random-access mode
Walkaway time
1 hour minimum when the system is fully loaded with samples, reagents, and supplies
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
Auto-reflex testing
User-defined automatic reflex testing
Sample carryover prevention
Disposable pipette tips eliminate sample carryover
Sample volume per test
10–300 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
5 mL, 7 mL, 10 mL, 1 mL sample cups, microtainer tubes
Sample capacity
84 sample continuous loading in 12 position sample racks
Pipette tips
ADVIA Centaur type; 480 onboard, automatic tracking and notification
STAT handling
Dedicated STAT position; additional keyboard option for scheduling STATs individually
Reaction area
Reaction cuvettes
Onboard capacity of 400 ADVIA Centaur cuvettes
Assay times
About 20–30 minutes,* assay-dependent
Assay technology
Direct chemiluminescence testing methodology using advanced acridinium ester technology
Reagent handling
Primary ancillaries
15-position cooled storage with refrigeration at 10–12°C (50–54°F)
Reagent ancillaries
10-position cooled storage with refrigeration at 10–12°C (50–54°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
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
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 results storage
25,000 control, patient, and event results can be stored in the database
Maintenance
Daily
Automated: ≤30 minutes; hands-on: <5 minutes
Weekly
Hands-on: ≤30 minutes
Monthly
Hands-on: ≤60 minutes
User interface/data management
Monitor
19-inch diagonal LCD touchscreen
Operating system
MICROSOFT WINDOWS 7
Remote access and service
Smart Remote Services
General specifications
Power requirements
100–240 V, 50/60 Hz
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: <1000 CFU/mL
Maximum resistivity: 1.0 megohm/cm
Drain requirements
7.5 L waste bottle (assembly is included)
Dimensions
81 (h) x 107 (w) x 74 (d) cm
32 (h) x 43 (w) x 29 (d) inches
(excluding monitor and accessories)
Weight
166 kg (366 lb) (including monitor and accessories)
Compliance
Complies with international environmental, health, and safety standards, including CE and RoHS
Noise emission
Up to 65 dB (with normal use)
Ambient temperature
18–30°C (64–90°F)
Ambient humidity
20–85% RH 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