Dimension Vista 500 Intelligent Lab System
The Dimension Vista® 500 System provides intelligent analytics where sample-centric design, unique integration of four technologies, including LOCI® advanced chemiluminescence, customer-driven engineering and flexibility of configurations all come together for a more efficient workflow.
- Sample-centric design incorporates Lean principles for simplified, consolidated sample processing
- Unique integration of four technologies allows simultaneous processing of tests for multiple disease states on a single platform from a single tube
- Customer-driven engineering helps eliminate many manual tasks freeing up technical time to address critical issues throughout the lab
- Flexibility of configurations to meet your laboratory needs today and into the future
Características e Benefícios
Unique integration of four technologies for speed and quality without compromise
Processes more than 100 assays simultaneously
- 144 onboard reagent slots
- Over 90% of typical lab testing processed on a single platform
- Disease state management from a single primary sample container
- Capacity for 600-800 samples onboard simultaneously
- Processes up to 1000 tests per hour
- Common reagent area and packaging
LOCI Advanced Chemiluminescence for trusted results in a Flash
- High sensitivity immunoassays integrated with fast turnaround time
♦ 10-minute cardiac panel
♦ 16-minute 3rd generation TSH
- The advanced homogeneous chemiluminescent technology
- Short reaction times with no wash or separation steps
- Low sample volumes
Customer-driven engineering helps eliminate manual tasks
- Consolidated testing
- Ease of use
- Automated hands-off calibration and QC
- Auto-sensitivity, precision and linearity
- Customizable QC and calibration auto-acceptance parameters
- Continual monitoring of onboard inventory
- Autoverification of results performed according to user-programmable rules
- Automatic repeat of panic values to ensure result reliability
- Dual sample clot-check; short-sample detect; sample quality management; sample integrity; serum indices (HIL)
- Onboard help system
- Onboard water purification module
"Vista® was worth the wait. It was critical to the quality of results to have access to new technology. LOCI® tests are great!"
Sacred Heart St. Mary's Hopsital
Rhinelander, WI
Sacred Heart St. Mary's Hopsital
Rhinelander, WI
"In comparison to the competitors, the Vista® footprint is great. It does so much in our small lab. The speed of the installation exceeded our expectations, and Siemens support was excellent."
Director, Alegent Health
Omaha, Nebraska
Director, Alegent Health
Omaha, Nebraska
"The Vista® 500 is faster than our existing systems."
Chemistry Supervisor
John Randolph Medical Center
Hopewell, VA
Chemistry Supervisor
John Randolph Medical Center
Hopewell, VA
"The system has very low maintenance".
"It was genius to put liquids under separate lock and key."
Assays
Anemia
Ferritin
Folate
Vitamin B12
Cardiac
BNP*
CKMB (Activity)
CKMB (Mass)
CardioPhase® hsCRP
Myoglobin
NT-proBNP
High-Sensitivity Troponin I
Diabetes
Fructosamine*,†
Hemoglobin A1c‡
Drugs of Abuse/Toxicology
Acetaminophen
6-Acetylmorphine (6-AM)§
Amphetamines
Barbiturates, Urine
Barbiturates, Serum§
Benzodiazepines, Urine
Benzodiazepines, Serum§
Buprenorphine§
Cannabinoids (THC)
Cocaine Metabolite
Ecstasy
EDDP (Methadone Metabolite)†
Ethyl Alcohol
Ethyl Glucuronide (EtG)†,**
Fentanyl†
Methadone
Methaqualone§
Opiates
Oxycodone
Phencyclidine
Propoxyphene§
Salicylate
Tramadol†
Tricyclic Antidepressants§
General Chemistry
Alanine Aminotransferase (ALT)
Albumin (BCP)
Albumin (Nephelometry)
Aldolase*,†
Alkaline Phosphatase (ALP)
Ammonia
Amylase
Aspartate Aminotransferase
Bilirubin, Direct
Bilirubin, Total
Calcium (CPC)
Carbon Dioxide
Chloride
Cholesterol
Creatine Kinase
Creatinine
Creatinine (Enzymatic)
Gamma Glutamyltransferase (GGT)
Glucose
Glucose, Hemolyzed*,§
HDL Cholesterol
Iron
Lactate
Lactate Dehydrogenase
LDL Cholesterol
Lipase
Magnesium
Microalbumin
Pancreatic Amylase*†
Phosphorus
Potassium
Pseudocholinesterase
Sodium
Total Iron Binding Capacity
Total Protein
Total Protein, CSF/Urine
Triglycerides
Urea Nitrogen (BUN)
Uric Acid
Immunosuppressant Drugs
Cyclosporine‡
Cyclosporine (Extended Range)‡
Inflammation
Total IgE
Metabolic
Homocysteine
Oncology
AFP
CA 125II
CA 15-3
CA 19-9
CEA
Free PSA
Total PSA
Reproductive Endocrinology
Estradiol
FSH
hCG
LH
Progesterone
Prolactin
Testosterone
Special Infectious Disease
SARS-COV-2 IgG††
SARS-COV-2 Total††
Specific Proteins
α1-Acid Glycoprotein
α1-Antitrypsin
α1-Microglobulin
α2-Macroglobulin
ß-2 Microglobulin
Antistreptolysin O (ASO)
Apolipoprotein A-I
Apolipoprotein B
C1 Inhibitor
Ceruloplasmin
Complement C3
Complement C4
CRP
Cystatin C
Haptoglobin
Hemopexin
Ig Light Chains, Type Kappa
Ig Light Chains, Type Lambda
IgG Subclass 1
IgG Subclass 2
IgG Subclass 3
IgG Subclass 4
Immunoglobulin A
Immunoglobulin E
Immunoglobulin G
Immunoglobulin M
Lipoprotein(a) Ultra*,†
Prealbumin
Retinol Binding Protein
Rheumatoid Factor (RF)
Soluble Transferrin Receptor (sTfR)
Transferrin
Therapeutic Drug Monitoring (TDM)
Amikacin§
Caffeine§
Carbamazepine
Digitoxin
Digoxin
Ethosuximide§
Gentamicin
Lamotrigine†
Levetiracetam†
Lidocaine
Lithium
Methotrexate†
N-Acetylprocainamide (NAPA)
Phenobarbital
Phenytoin
Procainamide
Theophylline
Tobramycin
Valproic Acid
Vancomycin
Thyroid
Free T3
Free T4
T Uptake
Total T4
TSH
Especificações Técnicas
* Not available for sale in the U.S.
† Alliance Application manufactured by third party, distributed by Siemens Healthcare Diagnostics.
‡ No manual pre-treatment.
§ Alliance Application manufactured and distributed by Siemens Healthcare Diagnostics.
** Restricted in the U.S. to law enforcement related use (forensic use only).
†† This test has not been FDA cleared or approved. This test has been authorized by 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 and is subject to regulatory requirements.