Official registry information on file with the National Plan and Provider Enumeration System.
PRODI LAB (NPI 1447843750) is a healthcare organization registered as a clinical medical laboratory in Pinecrest, Florida and active in the NPI registry since February 2021. The organization holds an CLIA Accreditation certificate valid through December 8, 2027, maintains a secondary practice location in Miami, and lists Anna A Mkhitarian, Authorized Person, as its authorized official.
NPPES Registry Identity
NPI1447843750
Entity TypeOrganization
Primary Taxonomy291U00000X
Legal Business NamePRO DIAMETRICS CORP
Location Address9627 S DIXIE HWYPinecrest, FL 33156-2804
(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.
The full list of accepted plans is on the Insurance tab. Issuers include Ambetter from Buckeye Health Plan, Ambetter from Meridian, Ambetter Health.Insurance ›
CLIA Laboratory Certificates CMS CLIA
Laboratory certificates issued under the Clinical Laboratory Improvement Amendments (CLIA) program, which sets federal quality standards for human laboratory testing in the United States. There is no official CMS crosswalk between CLIA and NPI numbers; these certificates are associated with this NPI by matching facility names, locations and phone numbers in the CMS CLIA registry.
CLIA data matches this NPI record on: ✓ Address✓ Name✓ Phone
This is a certificate that is issued to a laboratory on the basis of the laboratory's accreditation by an accreditation organization approved by CMS.
Areas of Expertise CMS Part B claims84
Services this provider delivered to Medicare fee-for-service patients, from the CMS Medicare utilization data. Higher counts generally reflect more experience with a service; care delivered outside Medicare is not included.
Detection test by nucleic acid for organism, amplified probe technique 87798
A nucleic acid detection test is a procedure to identify specific organisms in your body. This test uses an amplified probe technique, which magnifies the genetic material of the organism, making it easier to detect. It's a precise way to diagnose infections.
7,217 services902 patients
Gene analysis (phospholipase c gamma 2) for common variants 81320
Gene analysis for phospholipase C gamma 2 common variants is a test that checks for changes in the PLCG2 gene. These changes can sometimes lead to certain health conditions. The test uses a sample of your body's cells to analyze your DNA.
Gene analysis, specifically neurotrophic receptor tyrosine kinase 1 (NTRK1) translocation analysis, is a test that examines your genes for specific changes. These changes could potentially lead to certain health conditions. This analysis helps in providing personalized treatment plans.
2,877 services2,591 patients
Identification of organisms by genetic analysis, amplified probe technique 87150
This procedure involves identifying organisms like bacteria or viruses in your body. It's done by amplifying a small part of their genetic material, making it easier to detect. This technique helps in accurate diagnosis and appropriate treatment.
2,500 services191 patients
Gene analysis (phosphatase and tensin homolog), full sequence analysis 81321
Gene analysis, specifically phosphatase and tensin homolog (PTEN) full sequence analysis, is a test that looks at your DNA to identify any changes in the PTEN gene. This gene helps control cell growth and division. Changes may lead to certain health conditions.
2,380 services2,351 patients
Gene analysis for cancer (neuroblastoma) 81311
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.
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.
Gene analysis for RUNX1 involves studying a specific part of your DNA. This test helps identify changes or mutations in the RUNX1 gene, which can provide insights into certain health conditions. It's like reading a book to find any spelling mistakes that could change the story.
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.
Gene analysis of telomerase reverse transcriptase (TERT) involves studying a specific segment of your DNA. It helps understand how your body's cells age and multiply, which can be crucial in diagnosing and managing certain health conditions.
1,737 services1,731 patients
Gene analysis (bruton's tyrosine kinase) for common variants 81233
Gene analysis of Bruton's Tyrosine Kinase (BTK) for common variants is a test that examines your BTK gene. This gene plays a crucial role in the immune system. By studying it, we can identify any variations that might be linked to certain health conditions.
Gene analysis for the coagulation factor V Leiden variant is a test to identify a specific genetic mutation. This mutation can increase the risk of developing abnormal blood clots in veins. The test involves analyzing a sample of your DNA, usually taken from a blood sample.
1,684 services1,684 patients
Gene analysis (transforming growth factor beta-induced) for common variants 81333
Gene analysis for common variants in the transforming growth factor beta-induced (TGFBI) gene helps understand your genetic makeup better. This procedure checks for variations in the TGFBI gene, which can influence your health. It's a safe, non-invasive test that uses a simple blood or saliva sample.
1,633 services1,627 patients
Gene analysis (partner and localizer of brca2) full sequence analysis 81307
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.
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.
Gene analysis for the p.Leu265Pro variant involves studying the MYD88 gene, which plays a crucial role in immune response. This test helps identify changes in this gene that could potentially cause health issues. It's a non-invasive procedure, done through a blood sample.
1,628 services1,624 patients
Gene analysis (septin9) for promoter methylation 81327
Gene analysis (Septin9) for promoter methylation is a non-invasive procedure that examines your DNA to identify certain changes or abnormalities. This specific test focuses on the Septin9 gene, which, when altered, may indicate a higher risk for certain health conditions.
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.
1,619 services1,613 patients
Gene analysis (coagulation factor ix) full sequence analysis 81238
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.
1,609 services1,609 patients
Gene analysis (inhibitor of kappa light polypeptide gene enhancer in b-cells, kinase complex-associated protein) common variants 81260
Gene analysis for common variants in the IKBKAP gene helps understand your body's response to certain medications. This non-invasive test studies your DNA to identify variations in this gene, which can influence drug effectiveness and safety.
1,597 services1,597 patients
Gene analysis (glucose-6-phosphate dehydrogenase) full sequence analysis 81249
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.
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.
1,570 services1,570 patients
Gene analysis (glucose-6-phosphatase, catalytic subunit) common variants 81250
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.
1,565 services1,565 patients
Gene analysis (fanconi anemia, complementation group c) common variant 81242
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.
1,564 services1,564 patients
Detection test by nucleic acid for multiple types influenza virus 87502
A detection test by nucleic acid for multiple types of influenza virus is a diagnostic procedure. It identifies the genetic material of the virus in your body. It's highly accurate and can distinguish between different flu strains, helping in prompt and precise treatment.
1,507 services757 patients
Test for detecting nucleic acid of organism causing infection of central nervous system 87483
This test detects the genetic material (nucleic acid) of the organism causing an infection in the central nervous system. It helps to identify the specific cause of the infection, enabling precise treatment. The procedure involves collecting a sample, usually through a spinal tap, and analyzing it in a lab.
1,499 services753 patients
Detection test by nucleic acid for chlamydia pneumoniae, amplified probe technique 87486
This test checks for the presence of Chlamydia pneumoniae, a bacterium that can cause respiratory infections. It uses an amplified probe technique, which magnifies the bacterium's genetic material for easier detection. It's a standard, non-invasive procedure.
1,499 services753 patients
Detection test by nucleic acid for legionella pneumophila (water borne bacteria), amplified probe technique 87541
A detection test for Legionella Pneumophila, a waterborne bacteria, uses the amplified probe technique. This involves identifying the bacteria's unique genetic material (nucleic acid) and amplifying it for easier detection, aiding in accurate diagnosis.
1,499 services753 patients
Detection test by nucleic acid for mycoplasma pneumoniae (bacteria), amplified probe technique 87581
This test checks for Mycoplasma pneumoniae, a bacteria that can cause lung infection. It uses a method called amplified probe technique, which identifies the bacteria's genetic material. This helps in diagnosing the infection accurately.
1,499 services753 patients
Detection test by nucleic acid for enterovirus (intestinal virus), amplified probe technique 87498
This test identifies the presence of an enterovirus, a type of virus that primarily targets the digestive system. It uses a method called the amplified probe technique to boost the detection of the virus's genetic material, or nucleic acid.
1,498 services753 patients
Detection test by nucleic acid for multiple types of respiratory virus, multiple types or subtypes, 3-5 targets 87631
This test identifies different respiratory viruses by examining their nucleic acid, the building blocks of their genetic material. It can detect multiple types or subtypes, specifically 3-5 targets. This helps in diagnosing your respiratory illness accurately.
1,492 services747 patients
Detection test by nucleic acid for staphylococcus aureus (bacteria), amplified probe technique 87640
A detection test for Staphylococcus aureus uses a method called the amplified probe technique. This method identifies the bacteria's unique genetic material, or nucleic acid, helping to confirm its presence. It's a highly accurate way to detect this type of bacteria.
1,466 services727 patients
Gene analysis (hemochromatosis) common variants 81256
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.
Gene analysis, specifically neurotrophic receptor tyrosine kinase 2 (NTRK2) translocation analysis, is a test that studies alterations in your genes. This analysis helps identify changes in the NTRK2 gene, which can sometimes be linked to certain health conditions. It's a vital part of personalized medicine.
1,245 services1,222 patients
Gene analysis (poly[a] binding protein nuclear 1) for abnormal alleles 81312
Gene analysis for Poly(A) Binding Protein Nuclear 1 (PABPN1) checks for abnormal alleles or variations in your DNA. This test can help identify genetic disorders caused by these variations. It's a non-invasive procedure, involving a simple blood or saliva sample.
1,235 services1,234 patients
Gene analysis (partner and localizer of brca2) targeted sequence analysis 81309
Gene analysis, specifically the partner and localizer of BRCA2 targeted sequence analysis, is a scientific procedure that studies specific parts of your DNA. It helps to identify if you have certain genetic changes that may increase your risk of developing specific health conditions.
1,161 services1,156 patients
Gene analysis (ataxin 7) for abnormal alleles 81181
Gene analysis for ataxin 7 involves studying your DNA to identify any unusual changes in the ataxin 7 gene. These changes, known as abnormal alleles, can cause health conditions like spinocerebellar ataxia. The test helps in early detection and management.
1,121 services1,119 patients
Gene analysis (5, 10-methylenetetrahydrofolate reductase) common variants 81291
Gene analysis for 5,10-methylenetetrahydrofolate reductase (MTHFR) common variants is a test that looks at your DNA to identify any changes in the MTHFR gene. These changes can affect how your body processes certain vitamins, which could impact your overall health.
1,121 services1,119 patients
Gene analysis (additional sex combs like 1, transcriptional regulator) full sequence analysis 81175
Gene analysis, specifically of the Additional Sex Combs Like 1, is a process where your DNA is examined to identify changes or alterations in a particular gene. This analysis helps to understand certain health conditions better and can guide treatment decisions.
1,105 services1,105 patients
Gene analysis (atropin 1) for abnormal alleles 81177
Gene analysis for Atropin 1 involves studying your DNA to identify any unusual genetic variations. This test helps in understanding your genetic makeup better, which can aid in diagnosing or predicting certain health conditions.
1,102 services1,102 patients
Gene analysis (enhancer of zeste 2 polycomb repressive complex 2 subunit) of full sequence 81236
Gene analysis of the full sequence of the Enhancer of Zeste 2 Polycomb Repressive Complex 2 Subunit (EZH2) involves examining this specific gene in detail. This gene plays a crucial role in cell growth and division. The analysis helps identify any mutations that could potentially lead to health issues.
1,102 services1,102 patients
Gene analysis (huntingtin) for abnormal alleles 81271
Gene analysis for huntingtin examines your DNA to identify if you have abnormal versions of the huntingtin gene. These abnormal genes are associated with Huntington's disease, a nervous system disorder. This test helps in early detection and management.
1,101 services1,101 patients
Gene analysis (ataxin 1) for abnormal alleles 81178
Gene analysis of ataxin 1 involves studying your DNA to identify any abnormal versions of the ataxin 1 gene. This gene is associated with certain neurological disorders. The test helps in early detection and management of these conditions.
1,099 services1,099 patients
Gene analysis (ataxin 2) for abnormal alleles 81179
Gene analysis for ataxin 2 checks for alterations in the ATXN2 gene. This gene is responsible for producing a protein essential for normal cell functions. If abnormal, it may lead to certain neurological disorders. The test involves analyzing your DNA, typically obtained via a blood sample.
1,099 services1,099 patients
Gene analysis (ataxin 3) for abnormal alleles 81180
Gene analysis for ataxin 3 helps identify abnormal alleles, or variations, in the ataxin 3 gene. This gene plays a role in neurological function. If abnormal, it may indicate conditions like Machado-Joseph disease. The process involves analyzing a blood sample.
Gene analysis for ataxin 8 opposite strand checks for unusual gene variants. This test helps identify genetic conditions that could affect your health. It involves analyzing your DNA, usually from a blood sample, to find these abnormal alleles.
1,099 services1,099 patients
Gene analysis (ataxin 10) for abnormal alleles 81183
Gene analysis for ataxin 10 involves examining your DNA to identify any abnormal versions of the ataxin 10 gene. These abnormalities could potentially cause certain health conditions. This test is non-invasive and helps in early detection and management of these conditions.
1,099 services1,099 patients
Gene analysis (survival of motor neuron 1, telomeric) for dosage/deletion 81329
Gene analysis for survival of motor neuron 1 (SMN1) involves studying your DNA to identify changes or deletions in the SMN1 gene. This gene plays a key role in motor neuron health. Alterations can lead to conditions like spinal muscular atrophy. The process is safe and non-invasive.
Gene analysis for the protein phosphatase 2 regulatory subunit Bbeta checks for unusual variations in your genes. This helps to identify potential health issues related to these genes. It's a simple, non-invasive test using a blood or saliva sample.
1,099 services1,099 patients
Gene analysis (tata box binding protein) for abnormal alleles 81344
Gene analysis for the TATA box binding protein checks for abnormal alleles or variations in your DNA. This analysis helps identify potential genetic conditions. It's done by examining a sample of your cells, typically obtained through a blood draw or a cheek swab.
1,099 services1,099 patients
Gene analysis (fragile x intellectual disability 2) for detection of abnormal alleles 81171
Gene analysis for Fragile X Mental Retardation 2 involves studying your genetic material to identify any unusual changes in a specific gene. This can help determine if you have a particular genetic condition, or if you might pass it on to your children.
1,097 services1,097 patients
2019-ncov coronavirus, sars-cov-2/2019-ncov (covid-19), any technique, multiple types or subtypes (includes all targets), non-cdc U0002
This refers to a test for COVID-19, caused by the SARS-CoV-2 virus. The test identifies multiple types or subtypes of the virus, including all targets. It's not specifically based on the CDC's testing protocol. It helps determine if you're currently infected with the virus.
1,095 services299 patients
Gene analysis (peripheral myelin protein 22), duplication or deletion analysis 81324
Gene analysis of peripheral myelin protein 22 involves studying a specific gene linked to nerve function. This test identifies if there are any duplications or deletions in this gene, which could impact nerve health. This information helps in diagnosing certain neurological conditions.
1,094 services1,094 patients
Gene analysis (fragile x syndrome, x-linked intellectual disability) for detection of abnormal alleles 81243
Gene analysis for Fragile X Mental Retardation involves studying your DNA to identify any abnormal changes or 'alleles'. This helps in detecting the presence of Fragile X syndrome, a genetic condition that can cause learning and behavioral challenges.
1,092 services1,092 patients
Gene analysis (glucosidase, beta, acid) common variants 81251
Gene analysis of common variants in the beta-glucosidase acid enzyme helps understand certain health conditions. This enzyme plays a key role in the body's metabolism. By studying its variants, doctors can better diagnose and treat metabolic disorders.
1,083 services1,083 patients
Detection test for candida species (yeast), amplified probe technique 87481
This test helps identify Candida, a type of fungus often present in the human body. An amplified probe technique is used, which enhances detection of the fungus in a sample. This method increases the accuracy of the test, helping to determine the best treatment.
395 services259 patients
Detection test by nucleic acid for staphylococcus aureus, methicillin resistant (mrsa bacteria), amplified probe technique 87641
A detection test by nucleic acid for MRSA bacteria uses an amplified probe technique. It's a lab procedure that identifies the presence of MRSA, a type of bacteria resistant to many antibiotics. This test helps in deciding the best treatment.
351 services270 patients
Detection test by nucleic acid for vancomycin resistance strep (vre), amplified probe technique 87500
The detection test by nucleic acid for vancomycin-resistant strep (VRE) is a laboratory procedure. It uses an amplified probe technique to identify specific genetic material in bacteria. This helps determine if the bacteria are resistant to the antibiotic vancomycin.
343 services264 patients
Detection test by nucleic acid for strep (streptococcus, group a), quantification 87652
A detection test by nucleic acid for Group A Strep is a diagnostic procedure that identifies the presence and quantity of streptococcus bacteria in your body. This test uses a sample, usually a throat swab, to detect the bacteria's genetic material. It helps in diagnosing infections like strep throat.
340 services258 patients
Gene analysis (v-ki-ras2 kirsten rat sarcoma viral oncogene) variants in codons 12 and 13 81275
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.
302 services293 patients
Genomic sequence analysis panel for severe inherited conditions with sequencing of 15 or more genes 81443
This procedure involves analyzing your genetic material to identify specific mutations that could cause severe inherited conditions. It examines 15 or more genes. The information can help in diagnosis, treatment planning, and understanding your risk for certain diseases.
248 services248 patients
Gene analysis (calcium voltage-gated channel subunit alpha1 a) of full sequence 81185
Gene analysis of the calcium voltage-gated channel subunit alpha1 a involves examining your DNA to understand how your body regulates calcium. This helps identify potential health risks related to calcium imbalances. It's a non-invasive procedure involving a simple blood or saliva sample.
184 services182 patients
Gene analysis (methyl cpg binding protein 2) full sequence analysis 81302
Gene analysis, specifically Methyl CpG Binding Protein 2 (MECP2) full sequence analysis, is a detailed examination of your DNA. This test focuses on the MECP2 gene, which plays a crucial role in nerve cell function and development. The results can help identify alterations or mutations that may cause certain health conditions.
171 services169 patients
Gene analysis (epidermal growth factor receptor), common variants 81235
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.
141 services141 patients
Gene analysis (janus kinase 2) variant 81270
Gene analysis (Janus Kinase 2 variant) is a test that examines your DNA to identify any changes in the JAK2 gene. This gene is crucial for blood cell production. If it's mutated, it can lead to various blood disorders. The test helps in diagnosing these conditions.
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.
138 services138 patients
Gene analysis panel for evaluation of genes associated with epilepsy 81419
A gene analysis panel for epilepsy evaluates specific genes linked to this condition. This test can help understand your epilepsy type and severity, potentially guiding treatment options. It involves a blood sample and lab analysis.
138 services138 patients
Gene analysis (tumor protein 53) full sequence analysis 81351
Gene analysis, specifically tumor protein 53 (TP53) full sequence analysis, is a test that examines the entire TP53 gene. This gene plays a key role in preventing cancer. If there are changes or mutations in this gene, it could lead to an increased risk of developing various types of cancer.
134 services134 patients
Gene analysis (sphingomyelin phosphodiesterase 1, acid lysosomal) common variants 81330
Gene analysis of sphingomyelin phosphodiesterase 1, acid lysosomal, involves studying specific variants in your genes. This helps understand your body's enzyme production, which can influence health conditions. It's a non-invasive procedure using a simple blood or saliva sample.
128 services128 patients
Gene analysis (serpin peptidase inhibitor, clade a, alpha-1 antiproteinase, antitrypsin, member 1) common variants 81332
Gene analysis for SERPINA1 common variants is a test that checks for changes in the SERPINA1 gene. This gene helps protect your lungs and liver from damage. Certain changes can lead to conditions like lung disease or liver problems. This test helps identify those changes.
128 services128 patients
Gene analysis (cystatin b) of full sequence 81189
Gene analysis of the full sequence of Cystatin B is a test that examines your DNA to identify any changes in the Cystatin B gene. This gene is linked to certain health conditions. The analysis helps in diagnosing and tailoring treatment plans.
Gene analysis for Connexin 30 involves studying your DNA to identify variations in the GJB6 gene. This gene helps produce a protein vital for cell communication. Detecting common variants can help understand certain health conditions.
Gene analysis of the Connexin 26 protein involves studying your DNA to understand your genetic makeup better. This protein plays a key part in your body's cell communication. By examining its full gene sequence, we can identify any genetic variations that might impact your health.
97 services96 patients
Gene analysis (adenomatous polyposis coli), full gene sequence 81201
Gene analysis of the adenomatous polyposis coli (APC) involves studying the entire sequence of the APC gene. This test helps identify mutations that could lead to conditions like familial adenomatous polyposis. The procedure is non-invasive and uses a blood sample.
85 services85 patients
Gene analysis (mutl homolog 1, colon cancer, nonpolyposis type 2) full sequence analysis 81292
Gene analysis, specifically for MUTL Homolog 1, linked to colon cancer, involves studying your DNA sequence. This helps identify any changes or mutations that might increase your risk of developing colon cancer. It's a preventive measure to manage potential health risks.
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.
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.
70 services70 patients
Gene analysis (muts homolog 2, colon cancer, nonpolyposis type 1) full sequence analysis 81295
Gene analysis (MUTYH) full sequence analysis is a test that examines your DNA to identify any changes linked to nonpolyposis colon cancer type 1. This can help determine your risk of developing this type of cancer.
69 services69 patients
Gene analysis (cytochrome p450, family 2, subfamily d, polypeptide 6) common variants 81226
Gene analysis of cytochrome P450 2D6 (CYP2D6) common variants involves studying specific genes to understand your body's ability to process certain medications. This can help tailor treatments to your unique genetic makeup, optimizing medication effectiveness and safety.
65 services65 patients
Test for detecting genes for disorders related to ashkenazi jews, genomic sequence analysis panel, at least 9 genes 81412
This test examines at least 9 genes to identify potential disorders associated with Ashkenazi Jewish heritage. By analyzing your genomic sequence, it can predict your risk for certain conditions, helping you make informed health decisions.
61 services61 patients
Gene analysis (cytochrome p450, family 2, subfamily c, polypeptide 19) common variants 81225
Gene analysis of cytochrome P450 2C19 common variants is a test that helps understand how your body processes certain medications. This can help your doctor tailor treatments specifically for you, improving their effectiveness and safety.
21 services21 patients
Gene analysis (cytochrome p450, family 2, subfamily c, polypeptide 9) common variants 81227
Gene analysis for cytochrome P450 2C9 common variants is a test to identify specific genetic variations. These variations can affect how your body processes certain medications, helping to determine the most effective and safe drug dosage for you.
20 services20 patients
Detection test by nucleic acid for strep (streptococcus, group a), amplified probe technique 87651
This test detects Group A Streptococcus bacteria in your body. It uses an amplified probe technique, which amplifies the bacteria's nucleic acid, making it easier to identify. This test helps diagnose conditions like strep throat or scarlet fever.
15 services14 patients
Detection test by nucleic acid for strep (streptococcus, group b), amplified probe technique 87653
A detection test by nucleic acid for Group B Strep uses an amplified probe technique. This test identifies the presence of Group B Strep bacteria in the body. It involves collecting a sample, usually a swab, which is then examined in a lab for the bacteria's genetic material.
15 services14 patients
Frequently Asked Questions NPPES & CMS
Common questions about this NPI record, answered from the official NPPES registry and CMS datasets shown on this page.
What is Pro Diametrics Corp's NPI number?
The NPI number for Pro Diametrics Corp is 1447843750. It was assigned to this organization in the NPPES registry on February 17, 2021. The provider is doing business as Prodi Lab.
Where is Pro Diametrics Corp located?
Pro Diametrics Corp is located at 9627 S Dixie Hwy, Pinecrest, FL 33156. The listed phone number is (305) 532-0005.
What is Pro Diametrics Corp's specialty?
The primary specialty registered for this NPI is Clinical Medical Laboratory with taxonomy code 291U00000X.
Does Pro Diametrics Corp hold a CLIA laboratory certificate?
Yes. A Certificate of Accreditation (number 10D2224368) is associated with this NPI, valid through December 8, 2027. CLIA certificates authorize laboratory testing under the federal Clinical Laboratory Improvement Amendments program.
What insurance does Pro Diametrics Corp accept?
Health plans from Ambetter Health, Ambetter from Buckeye Health Plan and Ambetter from Meridian list Pro Diametrics Corp as in-network in at least one marketplace plan. Coverage varies by plan and year; verify with the insurer or the provider before a visit.
When was this NPI record last updated?
The NPPES record for Pro Diametrics Corp was last updated on February 10, 2023. NPI Profile syncs weekly with the NPPES registry data releases published by CMS. This NPI record was last updated 3 years ago. If this record has changed at CMS more recently, you can request an on-demand re-check against the live CMS registry, directly from this page.
# Prodi Lab · NPI 1447843750
Clinical Medical Laboratory organization in Pinecrest, Florida. Organization record, active in the CMS NPPES registry since February 17, 2021.
## Identity
- **NPI:** 1447843750 (Entity type: Organization)
- **Enumerated:** February 17, 2021
- **Primary specialty:** Clinical Medical Laboratory · taxonomy 291U00000X
- **Legal business name:** Pro Diametrics Corp
- **Organization subpart:** No
- **Authorized official:** Anna Mkhitarian, AUTHORIZED PERSON
## Practice location
- **Address:** 9627 S DIXIE HWY, Pinecrest, FL 33156-2804
- **Phone:** (305) 532-0005 · **Fax:** (305) 406-9403
## Record status
- **NPPES last updated:** February 10, 2023
- **CLIA laboratory certificates:** 1 on file
---
Source: [NPI Profile](https://npiprofile.com/npi/1447843750) · Data from the CMS NPPES public registry.
# Prodi Lab · NPI 1447843750
Clinical Medical Laboratory organization in Pinecrest, Florida. Organization record, active in the CMS NPPES registry since February 17, 2021.
## Identity
- **NPI:** 1447843750 (Entity type: Organization)
- **Enumerated:** February 17, 2021
- **Primary specialty:** Clinical Medical Laboratory · taxonomy 291U00000X
- **Legal business name:** Pro Diametrics Corp
- **Organization subpart:** No
- **Authorized official:** Anna Mkhitarian, AUTHORIZED PERSON
## Practice location
- **Address:** 9627 S DIXIE HWY, Pinecrest, FL 33156-2804
- **Phone:** (305) 532-0005 · **Fax:** (305) 406-9403
## Record status
- **NPPES last updated:** February 10, 2023
- **CLIA laboratory certificates:** 1 on file
---
Source: [NPI Profile](https://npiprofile.com/npi/1447843750) · Data from the CMS NPPES public registry.