LABCARE
NPI 1811615198
Clinical Medical Laboratory in Dallas, TX

NPI Status: Active since August 22, 2022

Contact Information

13601 PRESTON RD STE 360E
DALLAS, TX
ZIP 75240
Phone: (972) 807-7600

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  • Organization
  • Clinical Medical Laboratory

About LABCARE

This page provides the complete NPI Profile along with additional information for Labcare, a provider established in Dallas, Texas operating as a Clinical Medical Laboratory. The healthcare provider is registered in the NPI registry with number 1811615198 assigned on August 2022. The practitioner's primary taxonomy code is 291U00000X. The provider is registered as an organization and their NPI record was last updated 4 years ago. The provider's former legal business name is Labcare, Llc. The authorized official of this NPI record is Hamdan Dajeh (Owner)

NPI
1811615198
Provider Legal Name
LABCARE
Other Organization Name
LABCARE, LLC
Other Name Type
Former Legal Business Name (4)
Entity Type
Organization
Location Address
13601 PRESTON RD STE 360E DALLAS, TX 75240
Location Phone
(972) 807-7600
Mailing Address
13601 PRESTON RD STE 360E DALLAS, TX 75240
Mailing Phone
(972) 807-7600
Is Sole Proprietor?
No
Is Organization Subpart?
No
Enumeration Date
08-22-2022
Last Update Date
09-01-2022
Code Navigator

Establishments like Labcare 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

HAMDAN DAJEH

Authorized Official Title
OWNER
Authorized Official Phone
(980) 228-8103

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.

Gene analysis (bloom syndrome, recq helicase-like)

Gene analysis for Bloom Syndrome involves studying the RECQ helicase-like gene. This gene is responsible for DNA repair. When it's not working properly, it can lead to Bloom Syndrome, a condition that increases the risk of developing various types of cancer.

This service was performed 865 times for 865 patients

Gene analysis (coagulation factor ix) full sequence analysis

Gene analysis for coagulation factor IX is a process that examines your genes, specifically the one responsible for factor IX - a protein that helps blood clot. It can detect any changes or mutations in this gene, which could affect your body's ability to control bleeding.

This service was performed 826 times for 826 patients

Gene analysis (cystic fibrosis transmembrane conductance regular) full gene sequence

Gene analysis for cystic fibrosis involves examining the entire CFTR gene to identify any changes or mutations that could cause the disease. This can help in diagnosing and managing the condition effectively.

This service was performed 882 times for 881 patients

Gene analysis (fanconi anemia, complementation group c) common variant

Gene analysis for Fanconi Anemia, Complementation Group C, is a test that looks at your DNA to see if you have changes in a specific gene linked to this type of anemia. This can help determine if you have the condition or if you might pass it on to your children.

This service was performed 848 times for 848 patients

Gene analysis (glucose-6-phosphatase, catalytic subunit) common variants

Gene analysis of glucose-6-phosphatase, catalytic subunit, common variants involves studying specific genes related to glucose metabolism. This helps understand if you're at risk of certain metabolic disorders. It's a non-invasive procedure, involving a simple blood or saliva sample.

This service was performed 894 times for 894 patients

Gene analysis (glucose-6-phosphate dehydrogenase) full sequence analysis

Gene analysis for glucose-6-phosphate dehydrogenase (G6PD) involves studying your DNA to check for changes in the G6PD gene. This gene controls an enzyme that helps red blood cells function properly. Anomalies can cause health issues like anemia.

This service was performed 884 times for 884 patients

Gene analysis (janus kinase 2) targeted sequence analysis

Gene analysis, specifically Janus Kinase 2 (JAK2) targeted sequence analysis, is a lab test that studies a specific gene in your body. It helps identify changes or mutations in the JAK2 gene, which can be linked to certain health conditions. This analysis is performed on a blood or bone marrow sample.

This service was performed 921 times for 920 patients

Gene analysis (mpl proto-oncogene, thrombopoietin receptor) sequence analysis of exon 10

Gene analysis of the MPL proto-oncogene, thrombopoietin receptor, specifically sequence analysis of exon 10, is a procedure that studies a specific part of your DNA. It helps to identify any changes or mutations that may contribute to certain blood disorders.

This service was performed 921 times for 920 patients

Gene analysis (muts homolog 2, colon cancer, nonpolyposis type 1) duplication or deletion variants

Gene analysis for MUTS homolog 2 (colon cancer, nonpolyposis type 1) duplication or deletion variants is a test that looks for changes in a specific gene linked to a higher risk of colon cancer. It helps identify if you carry these gene changes, aiding in early detection and prevention.

This service was performed 19 times for 19 patients

Gene analysis (muts homolog 6 [e coli]) duplication or deletion variants

Gene analysis (muts homolog 6 [e coli]) duplication or deletion variants is a genetic test. It identifies changes in your DNA that could indicate certain health conditions. This test looks specifically at the mutS homolog 6 gene for any duplications or deletions.

This service was performed 189 times for 189 patients

Gene analysis (muts homolog 6 [e coli]) full sequence analysis

Gene analysis, specifically MUTS Homolog 6 (E. coli) full sequence analysis, is a test that examines your DNA to identify changes in the MUTS Homolog 6 gene. This information helps doctors understand and manage potential health concerns.

This service was performed 813 times for 813 patients

Gene analysis (partner and localizer of brca2) full sequence analysis

Gene analysis, specifically for the partner and localizer of BRCA2, involves examining your genetic code to identify any changes in this particular gene. This gene is significant in maintaining the health of your cells. The full sequence analysis means we look at every part of this gene to ensure it's working properly.

This service was performed 1,022 times for 1,021 patients

Gene analysis (postmeiotic segregation increased 2 [s cerevisiae]) duplication or deletion variants

Gene analysis for PMS2 duplication or deletion variants involves studying your DNA to detect changes in the PMS2 gene. This gene is important for DNA repair. Variations in this gene could potentially lead to certain health conditions. This test helps to identify these changes early.

This service was performed 189 times for 189 patients

Gene analysis (postmeiotic segregation increased 2 [s cerevisiae]) full sequence analysis

Gene analysis, specifically postmeiotic segregation increased 2 (s cerevisiae) full sequence analysis, is a scientific procedure. It involves studying your entire genetic code to identify any changes or differences that could be related to certain health conditions. This is done in a lab, using a sample provided by you.

This service was performed 955 times for 955 patients

Test for detecting genes associated with colon cancer, genomic sequence analysis panel, at least 10 genes

This is a genetic test that checks for specific genes linked to colon cancer. The test analyzes a minimum of 10 genes to identify any changes or mutations that may increase the risk of developing this type of cancer.

This service was performed 194 times for 194 patients

Test for detecting genes associated with inherited breast cancer-related disorders

This test identifies if you carry certain genes linked to inherited disorders related to breast health. It's done through a simple blood or saliva sample. Results can help determine your risk and guide future health decisions.

This service was performed 184 times for 184 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 1811615198, we treat the final digit (8) 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 52. The final step is to find the difference between that total and the next multiple of ten (60 - 52 = 8).

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
1
Doubled → 2
Pos 4
1
Unchanged
Pos 5
6
Doubled → 12 → 1 + 2
Pos 6
1
Unchanged
Pos 7
5
Doubled → 10 → 1 + 0
Pos 8
1
Unchanged
Pos 9
9
Doubled → 18 → 1 + 8
Check
8
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 1 → 2 6 → 12 → 3 5 → 10 → 1 9 → 18 → 9

Step 2: Add all digits plus the NPI constant

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

2 + 8 + 2 + 1 + 1 + 2 + 1 + 1 + 0 + 1 + 1 + 8 + 24 = 52

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

The next multiple of ten after 52 is 60. The difference is the calculated check digit.

60 - 52 = 8
This NPI is valid
The calculated check digit is 8, which matches the last digit of 1811615198.

Other Providers at the Same Location


The following 2 providers are registered at the same or a nearby location.

Clinical Medical Laboratory
13601 PRESTON RD STE 360E
DALLAS, TX 75240
Clinical Medical Laboratory
13601 PRESTON RD STE 360E
DALLAS, TX 75240

Frequently Asked Questions

The NPI number assigned to this healthcare provider is 1811615198, enumerated as an "organization" on August 22, 2022.

The provider is located at 13601 PRESTON RD STE 360E DALLAS, TX 75240 and the phone number is (972) 807-7600.

Clinical Medical Laboratory with taxonomy code 291U00000X.