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  1. Siemens Healthineers Türkiye
  2. Laboratuvar Diagnostiği
  3. Immunoassay
  4. Immunoassay Sistemleri
  5. ADVIA Centaur XP İmmünoassay Sistemi
ADVIA Centaur XP Immunoassay System

ADVIA Centaur XP İmmünoassay Sistemi

Laboratuvarınız çeşitli test taleplerini nasıl karşılıyor?

Laboratuvarınız, verimlilikten ödün vermeden hem rutin hem de özel testleri gerçekleştirebilir mi? Giderek artan çeşitlilikteki hasta popülasyonu için hızı ve doğruluğu koruyabilir misiniz? Yüksek performanslı ADVIA Centaur® XP sistemi, hacim veya test türlerinden bağımsız olarak üretkenliği en üst düzeye çıkarmak için daha fazla yerleşik reaktife ve özel STAT özelliklerine sahiptir. Her zaman hazırdır ve kesintisiz çalışır.

  • Saatte 240 teste kadar yüksek verim 
  • Kullanım kolaylığı için sezgisel yazılım 
  • STAT bağlantı noktası, herhangi bir zamanda öncelikli örneklemeyi garanti eder 
  • Veri arşivi, idari görevleri azaltır 
  • 30 yerleşik reaktif içeren kapsamlı menü 
  • Siemens' Aptio™ Otomasyonu, ADVIA® Otomasyonu, StreamLAB® Otomasyonu veya VersaCell® Çözümlerine bağlanarak üretkenliği artırın 

Özellikler ve Faydalar

Immunodiagnostics at a Higher Level
Immunodiagnostics at a Higher Level
Comprehensive Menu

Kapsamlı Menü 

  • Kapsamlı teşhis testleri, tarama, teşhis, risk değerlendirmesi ve izlemeyi kapsar
  • 30 yerleşik reaktif, test kapasitesini en üst düzeye çıkarır

Powerful Productivity

Powerful Productivity

  • High throughput, up to 240 tests per hour, to keep pace with peak workload times
  • High-resolution touch screen for easy interaction
  • Expanded ancillary reagent and fluid capacity
  • Data archive feature reduces time for administrative tasks
  • Universal sample rack design eliminates manual tasks
Excellent Patient Care

Mükemmel Hasta Bakımı 

  • STAT bağlantı noktası, herhangi bir zamanda öncelikli örneklemeyi garanti eder 
  • Tek kullanımlık pipet uçları, numuneden numuneye bulaşmayı ortadan kaldırır 
  • Otomatik seyreltme, tekrarlama ve refleks testi Akıllı Algoritma Yazılımı, reaktif testi otomatik olarak tekrarlar ve onaylar 

Superior Service

Üstün Hizmet

  • 360º durum ışığı, tüm noktalardan görülebilen sistem bilgilerini görüntüler
  • Kullanıcı arayüzü, özelleştirilmiş ergonomi için ayarlar
  • Otomatik bakım özellikleriyle günlük başlatma yok
  • Yeni cihaz sensörleri, uzaktan teşhis fonksiyonlarını geliştiriyor

Esnek Çözümler 

  • Aptio™ Otomasyonu, ADVIA® Otomasyonu, StreamLAB® Otomasyonu ve VersaCell® Çözümlerine Bağlantı 
  • Siemens Healthineers Remote Service (SRS), Siemens Healthineers sistemlerinin proaktif olarak bakımını yapıyor 

Ölçümler

Anemia
Active B12
EPO
Ferritin
Folate
RBC Folate
Vitamin B12

Autoimmune
Anti-CCP IgG

Bone Metabolism
Intact PTH
Vitamin D Total

Cardiac
BNP
CKMB
High-Sensitivity Troponin I
Myoglobin
NT-proBNP

Diabetes
C-Peptide
Insulin

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

HIV
HIV 1/0/2 Enhanced (EHIV)
HIV Ag/Ab Combo (CHIV)

Immunosuppressant Drugs
Cyclosporine
Everolimus*
Sirolimus*
Tacrolimus*

Inflammation
IgE Total
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)*
Total Tau (TTAU)*

Oncology
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)*

Reproductive Endocrinology
AFP
Androstenedione
Anti-Müllerian Hormone*
DHEA-SO4
Enhanced Estradiol
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 Ag (CoVAg)**
SARS-CoV-2 IgG (COV2G)§
SARS-CoV-2 IgG (sCOVG)**
SARS-CoV-2 Total (COV2T)§
Syphilis
Zika Test‡

Therapeutic Drug Monitoring
Carbamazepine
Digitoxin
Digoxin
Gentamicin
Phenobarbital
Phenytoin
Theophylline
Valproic Acid
Vancomycin

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
Toxoplasma IgM

Teknik Özellikler

Overview

 

System Description

Random access immunoassay system

Throughput

Up to 240 tests per hour

Time To First Result

18 minutes; results every 15 seconds thereafter, assay dependent

Assays On Board

30

Assay Packs

ADVIA Centaur® ReadyPack™ assays

Assay Technology

Direct Chemiluminescence using Acridinium Ester technology

Sample Handling

 

Sample Tubes

1 mL, 2 mL, 3 mL, 5 mL, 7 mL, 10 mL, micro container tubes

Sample Carriers

Universal 5-position rack holds multiple tube types; 180 samples fully loaded; no-pause loading and unloading

STAT Handling

Dedicated STAT port accepts samples any time

Sample Types

Serum, plasma, urine - assay dependent

Sample Volume

10 uL to 200 uL assay dependent

Sample Integrity Control

Pressure transducer technology with clot management, detection, and flagging.

Sample Pipette Tips

Ensure zero sample carryover

Automatic Dilutions

Varies by assay, up to 1:1000

Bar Codes

 

 

Code 128, Code 39, Codabar, Interleaved 2 of 5

Reagent Handling

 

Reagent Cooling

30-position reagent tray cooled 4°C to 8°C

Reagent Integrity Control

Barcode reagent identification, automatic inventory tracking and flagging, calibration validity tracked and flagged, reagent on board stability tracked and flagged, reagent expired/ reagent low flagging

Reagent Mixing

ReadyPacks automatically rocked onboard

Ancillary Reagents

25-position ancillary reagent tray cooled 4°C to 8°C

Supplies

 

Cuvettes

1,000 ADVIA Centaur cuvette capacity

Sample Tips

ADVIA Centaur type, 840 on board, automatic tracking, and flagging of inventory

Continuous Operation

 

 

Loading/unloading of samples and consumables at anytime without he need to interrupt system operations, includes: sample racks, STATS, reagent packs, ancillary reagent packs, reaction cuvettes, sample pipette tips, calibrators, controls, wash fluids, water, and waste.

User Interface

 

Monitor

19-inch diagonal high-resolution LCD touch screen with adjustable height

Operating System Results Management

Dual Sun Microsystems Sparc® II processors; Microsoft® Windows® XP

Host Interface

RS232C bidirectional and host query; Ethernet connection available; 25,000 result storage; archive to removable media; automatic reflex testing

Smart Algorithm Software

Repeats and confirms reactive testing; results available as completed

Quality Control

 

 

Advanced QC package includes Levy-Jennings plots and Westgard rules; 65,000 control results can be stored

Removable Media

 

 

DVD or CD-RW

Device Management

 

 

100 Base-T Ethernet port for remote access and Siemens Remote Service proactive service modem

General Specifications

 

Electrical

208-240 V at 50/60 Hz; meets regulatory requirements for UL, CAN/CSA, IEC1010. JIS, CE, CISPR11 Class A

Power Consumption

1 KW in ready state; 1.5 KW in operating state

Water

Deionized type II

Dimensions

51.5 (h) x 72.4 (w) x 41.0 (d) in-130.9 (h) x 183.9 (w) x 104.2 (d) cm

Weight

1,200 lbs (545 kg)

Floor Load-bearing Requirement

390 kg/m2 (80lb/ft2)

Operating Environment Temperature

18-30OC; humidity 20-80% noncondensing

Ventilation

10,000 BTU/hour

Noise Emission

58.8 db in ready state; 61.3 in operating state

* Under development. Not available for sale.

† CA 125II , CA 19-9 and CA 15-3 are trademarks of Fujirebio Diagnostics, Inc.

‡ Limited distribution.

§ This test has not been FDA cleared or approved. This test has been authorizedby FDA under an EUA for use by authorized laboratories. This test has been authorized only for detecting the presence of antibodies against SARS-CoV-2, not for any other viruses or pathogens. This test is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Act, 21 U.S.C. § 360bbb-3(b)(1), unless the authorization is terminated or revoked sooner. Product availability may vary by country. 

** This test has not been reviewed by the FDA. In the US, use of this test is limited to laboratories that are certified under Clinical Laboratory Improvement Amendments of 1988 (CLIA) to perform high-complexity testing. Product availability may vary by country and is subject to regulatory requirements.

The products/features (mentioned herein) are not commercially available in all countries. Due to regulatory reasons their future availability cannot be guaranteed. Please contact your local Siemens Healthineers organization for further details.