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  5. Dimension Vista 1500 Intelligent Lab System
Dimension Vista 1500 Intelligent Lab System

Dimension Vista 1500 Intelligent Lab System

This analyzer is no longer for sale in the U.S.

Revolutionize the way your lab functions with the new Dimension Vista® 1500 Intelligent Lab System. This new class of analyzer incorporates customer-driven design, ultra-integration of four technologies, including state-of-the-art LOCI® technology, and onboard automation.

  • Customer-driven design increases operational simplicity delivering the confidence that every trained technician can run any test any time
  • Ultra-integration of four technologies in one smart workstation increases productivity
  • LOCI advanced chemiluminescence produces trusted results in a flash
  • Automation onboard eliminates manual tasks and frees up technician’s time to address critical issues elsewhere in the laboratory

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

Technical Specifications

Weight

2,034 lb (922.61 kg)

Dimensions

Width: 84 ¾” (215.3 cm)

Height (without monitor): 55 ½” (141.2 cm)

Height (with cover open): 80 3/8” (204 cm)

Depth: 51 7/8” (131.7 cm)

* 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.

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.

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