UNIVERSITY PHYSICIANS, INCORPORATED
NPI 1861946360
Clinical Medical Laboratory in Aurora, CO

NPI Status: Active since August 12, 2016

Contact Information

12705 E MONTVIEW BLVD STE 400
COLORADO MOLECULAR CORRELATES LABORATORY
AURORA, CO
ZIP 80045
Phone: (303) 493-7000

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  • Organization
  • Clinical Medical Laboratory

About UNIVERSITY PHYSICIANS, INCORPORATED

This page provides the complete NPI Profile along with additional information for University Physicians, Incorporated, a provider established in Aurora, Colorado operating as a Clinical Medical Laboratory. The healthcare provider is registered in the NPI registry with number 1861946360 assigned on August 2016. The practitioner's primary taxonomy code is 291U00000X. The provider is registered as an organization and their NPI record was last updated one year ago. The provider's . The authorized official of this NPI record is Lisa Donahue (Associate Compliance Officer)

NPI
1861946360
Provider Legal Name
UNIVERSITY PHYSICIANS, INCORPORATED
Other Organization Name
Other Name Type
(6)
Entity Type
Organization
Location Address
12705 E MONTVIEW BLVD STE 400 COLORADO MOLECULAR CORRELATES LABORATORY AURORA, CO 80045
Location Phone
(303) 493-7000
Mailing Address
PO BOX 110429 AURORA, CO 80042
Mailing Phone
(303) 493-7000
Is Sole Proprietor?
No
Is Organization Subpart?
No
Enumeration Date
08-12-2016
Last Update Date
06-08-2025
Code Navigator

Establishments like University Physicians, Incorporated are healthcare facilities that may perform a wide range of laboratory procedures, assisted by doctors and medical technologists. Laboratories can be categorized according to their function as common diagnostic labs or specialty labs that conduct specialized or confirmatory tests. Different clinical laboratories could specialize in clinical chemistry, clinical microbiology, hematology, serology, clinical microscopy, cytopathology, molecular biology, or public health. Please inquire directly with this provider to confirm their test menu.

Location Map

Specialty - Primary Taxonomy

The NPI enumerator requires providers to submit at least one taxonomy code. A taxonomy code is a unique 10-character code that describes the healthcare provider type, classification, and the area of specialization. There could be only one primary taxonomy code per NPI record. For individual NPIs the license data is associated to the taxonomy code.

Classification

Clinical Medical Laboratory

Taxonomy Code
291U00000X
Type
Laboratories
Taxonomy Description
(1) A clinical laboratory is a facility for the biological, microbiological, serological, chemical, immunohematological, hematological, biophysical, cytological, pathological, or other examination of materials derived from the human body for the purpose of providing information for the diagnosis, prevention, or treatment of any disease or impairment of, human beings. These examinations also include procedures to determine, measure, or otherwise describe the presence or absence of various substances or organisms in the body. Facilities only collecting or preparing specimens (or both) or only serving as a mailing service and not performing testing are not considered clinical laboratories. (2) Any facility that examines materials from the human body for purposes of providing information for the diagnosis, prevention, or treatment of any disease or impairment of, or the assessment of, the health of human beings. Typical divisions of a clinical laboratory include hematology, cytology, bacteriology, histology, biochemistry, medical toxicology, and serology.

Authorized Official

The authorized official is the designated individual with the legal authority to make changes to the provider’s official NPI record. For organizations, the authorized official must be a general partner, chairman of the board, CEO, CFO or a direct owner holding at least a 5 percent stake in the medical organization.

Authorized Official Name

LISA DONAHUE

Authorized Official Title
ASSOCIATE COMPLIANCE OFFICER
Authorized Official Phone
(303) 493-7300

Areas of Expertise

The following services and procedures, recently provided to Medicare patients, illustrate the range of care this provider offers. This list reflects the variety of services available to all patients visiting the practice and is based on 2022 Medicare dataset. In general, the more frequently a provider treats specific conditions or performs particular procedures, the more experienced they become in addressing similar patient needs. The provider has delivered many of the services listed below to Medicare patients. Please note that this list does not include services provided to patients who are not covered by Medicare.

Chimerism analysis post transplantation, with cell selection

Chimerism analysis post-transplantation is a test done to monitor your body's acceptance of a transplanted organ or cells. It checks if the new cells are working well with your own. Cell selection helps to focus on specific cell types for a more detailed analysis.

This service was performed 20 times for 20 patients

Chimerism analysis post transplantation, without cell selection

Chimerism analysis post-transplantation is a test done to monitor the success of a bone marrow or stem cell transplant. It checks if the patient's body has accepted the new cells and if these cells are functioning properly. This version of the test does not involve specific cell selection.

This service was performed 24 times for 24 patients

Comparative analysis using short tandem repeat (str) markers of patient and specimen

Comparative analysis using STR markers is a technique to match DNA samples. It involves comparing specific regions of your DNA with a specimen's DNA. This helps to confirm if the DNA in the specimen belongs to you or not, ensuring accuracy in diagnosis and treatment.

This service was performed 15 times for 15 patients

Examination of archival tissue for genetic analysis

Examination of archival tissue for genetic analysis involves studying previously collected tissue samples. This process helps detect any genetic alterations that may be linked to certain diseases. It's a crucial step in understanding your health and planning appropriate treatments.

This service was performed 13 times for 12 patients

Gene analysis (epidermal growth factor receptor), common variants

Gene analysis of the epidermal growth factor receptor (EGFR) identifies common variants in this particular gene. This test helps in understanding your body's response to certain medications. It aids in personalized treatment planning, ensuring the most effective care.

This service was performed 58 times for 57 patients

Gene analysis (hemochromatosis) common variants

Gene analysis for hemochromatosis common variants is a test that checks for specific changes in your DNA. These changes could indicate a higher risk of developing hemochromatosis, a condition that causes your body to absorb too much iron from your diet.

This service was performed 30 times for 30 patients

Gene analysis (kirsten rat sarcoma viral oncogene homolog), additional variants

Gene analysis of the Kirsten rat sarcoma viral oncogene homolog (KRAS) checks for extra variations in the KRAS gene. These variations may impact how your body responds to certain treatments. It's a non-invasive test, usually done on a blood or tissue sample.

This service was performed 66 times for 65 patients

Gene analysis (neurotrophic receptor tyrosine kinase 1, 2, and 3) translocation analysis

Gene analysis for neurotrophic receptor tyrosine kinase (NTRK) 1, 2, and 3 translocation is a test that checks for changes in your genes. These changes can impact how cells grow and divide, which can affect your health. It's a way to catch problems early.

This service was performed 69 times for 67 patients

Gene analysis (v-ki-ras2 kirsten rat sarcoma viral oncogene) variants in codons 12 and 13

Gene analysis for v-ki-ras2 kirsten rat sarcoma viral oncogene variants in codons 12 and 13 is a test to identify specific changes in your genes. These changes could potentially indicate a higher risk for certain types of cancer.

This service was performed 69 times for 69 patients

Gene analysis (v-raf murine sarcoma viral oncogene homolog b1)

Gene analysis of v-raf murine sarcoma viral oncogene homolog b1 (BRAF) is a test that examines your DNA to identify changes or mutations in the BRAF gene. This information can help in diagnosing and treating certain diseases, including some types of cancer.

This service was performed 84 times for 84 patients

Gene analysis for cancer (neuroblastoma)

Gene analysis for neuroblastoma is a test that studies your genes to identify abnormalities linked to this type of cancer. It helps doctors tailor treatment plans, potentially improving outcomes and reducing side effects.

This service was performed 17 times for 17 patients

Microsatellite instability analysis

Microsatellite instability analysis is a test that checks for abnormalities in your DNA, which could indicate a higher risk for certain types of cancers. It is a useful tool for early detection and prevention.

This service was performed 19 times for 19 patients

Microscopic genetic analysis of tumor, manual

Microscopic genetic analysis of a tumor involves examining your tumor's genes under a microscope. This helps identify specific genetic changes in the tumor cells. This information can aid in diagnosing, predicting disease progression, and determining the most effective treatment options.

This service was performed 15 times for 15 patients

Molecular pathology procedure; physician interpretation and report

A molecular pathology procedure involves analyzing your body's cells at a molecular level to identify any abnormalities. This can help detect diseases early. A physician will interpret the results and provide a detailed report, explaining the findings clearly.

This service was performed 180 times for 137 patients

Preparation of specimen, manual

The preparation of a specimen manually is a procedure where a sample from your body is collected by a healthcare professional. This could be blood, urine, or tissue. The sample is then prepared in a lab for further analysis to help diagnose or monitor your health condition.

This service was performed 11 times for 11 patients

Test for detecting genes associated with cancer of body organ

This test identifies specific genes linked with body organ cancer. It's a simple process where a sample of your blood or saliva is collected. The sample is then analyzed in a lab to find any genetic changes that might increase cancer risk. It's a proactive step to manage your health.

This service was performed 133 times for 133 patients

Test for detecting genes associated with colon cancer, promoter methylation analysis

Promoter methylation analysis is a test that helps identify certain genes linked to colon cancer. This process examines how the DNA in your cells is modified, which can indicate if you're at risk for this type of cancer.

This service was performed 23 times for 23 patients

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NPI NPI Number Validation

How NPI Validation Works

The NPI validation process uses the ISO-standard Luhn algorithm, a mathematical "handshake", to ensure that a provider's 10-digit ID is authentic and free of common typing errors.

To verify the NPI 1861946360, we treat the final digit (0) as the Check Digit—the target answer we need to reach. The process begins by taking the first nine digits and adding a constant value of 24, which accounts for the "80840" prefix required for all U.S. health identifiers. We then double every other digit starting from the right and sum the individual digits of those results together. For this specific NPI, that total comes to 60. The final step is to find the difference between that total and the next multiple of ten (60 - 60 = 0).

Digit-by-digit view

Use the first nine digits for the calculation. Starting from the right, double every other digit. The last digit is the check digit and is not part of the calculation.

Pos 1
1
Doubled → 2
Pos 2
8
Unchanged
Pos 3
6
Doubled → 12 → 1 + 2
Pos 4
1
Unchanged
Pos 5
9
Doubled → 18 → 1 + 8
Pos 6
4
Unchanged
Pos 7
6
Doubled → 12 → 1 + 2
Pos 8
3
Unchanged
Pos 9
6
Doubled → 12 → 1 + 2
Check
0
Target digit
Regular digit Doubled digit Check digit

Step 1: Double every other digit from the right

Starting with the rightmost digit of the first nine digits, double every other value. If doubling creates a two-digit number, add those digits together.

1 → 2 6 → 12 → 3 9 → 18 → 9 6 → 12 → 3 6 → 12 → 3

Step 2: Add all digits plus the NPI constant

Add the transformed values, the unchanged digits, and the constant 24.

2 + 8 + 1 + 2 + 1 + 1 + 8 + 4 + 1 + 2 + 3 + 1 + 2 + 24 = 60

Step 3: Find the amount needed to reach the next multiple of 10

The next multiple of ten after 60 is 60. The difference is the calculated check digit.

60 - 60 = 0
This NPI is valid
The calculated check digit is 0, which matches the last digit of 1861946360.

Other Providers at the Same Location


The following 4 providers are registered at the same or a nearby location.

Medical Genetics, Ph.D. Medical Genetics
12705 E MONTVIEW BLVD STE 400
AURORA, CO 80045
Medical Genetics (Clinical Cytogenetics)
12705 E MONTVIEW BLVD STE 400
AURORA, CO 80045
Clinical Medical Laboratory
12705 E MONTVIEW BLVD STE 400, UC DENVER COLO GENETICS LAB (CYTO)
AURORA, CO 80045
Pathology (Clinical Laboratory Director, Non-physician)
12705 E MONTVIEW BLVD STE 400
AURORA, CO 80045

Frequently Asked Questions

The NPI number assigned to this healthcare provider is 1861946360, enumerated as an "organization" on August 12, 2016.

The provider is located at 12705 E MONTVIEW BLVD STE 400 COLORADO MOLECULAR CORRELATES LABORATORY AURORA, CO 80045 and the phone number is (303) 493-7000.

Clinical Medical Laboratory with taxonomy code 291U00000X.