SIPARADIGM LLC
NPI 1891909941
Clinical Medical Laboratory in Pine Brook, NJ

Q: What is Siparadigm LLC's NPI number?

The NPI number for Siparadigm LLC is 1891909941. It was assigned to this organization in the NPPES registry on May 9, 2007.

Q: What is Siparadigm LLC's specialty?

The primary specialty registered for this NPI is Clinical Medical Laboratory with taxonomy code 291U00000X.

Q: When was this NPI record last updated?

The NPPES record for Siparadigm LLC was last updated on March 30, 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.

Active since May 09, 2007CLIA 31D1028659 · Accreditation

25 RIVERSIDE DR STE 2, PINE BROOK, NJ 07058(201) 599-9044(201) 599-9066 Get Directions Write a Review

NPPES record last updated: March 30, 2023. Verified against the NPPES registry weekly; last sync: August 09, 2026.

Record update history: Mar 30, 2023, Jul 21, 2022, Jun 23, 2017 (3 updates tracked since 2017).

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About Siparadigm Llc NPPES

Official registry information on file with the National Plan and Provider Enumeration System.

SIPARADIGM LLC (NPI 1891909941) is a healthcare organization registered as a clinical medical laboratory in Pine Brook, New Jersey and active in the NPI registry since May 2007. The organization holds an CLIA Accreditation certificate valid through March 20, 2027 and lists Ruth Amicosante, Billing Manager, as its authorized official.

NPPES Registry Identity

NPI1891909941

Entity TypeOrganization

Primary Taxonomy291U00000X

Legal Business NameSIPARADIGM LLC

Location Address25 RIVERSIDE DR STE 2Pine Brook, NJ 07058-9391

Mailing Address25 Riverside Dr Ste 2Pine Brook, NJ 07058-9391 · (201) 599-9044 · Fax (201) 599-9066

Phone(201) 599-9044

Fax(201) 599-9066

Organization SubpartNo

Authorized OfficialRuth AmicosanteBilling Manager · (650) 395-9124

Enumeration DateMay 9, 2007

Last NPPES UpdateMarch 30, 20233 updates tracked since enumeration

NPPES CertifiedMarch 30, 2023

✔ NPI 1891909941 is a valid, active identifier and passes the ISO check-digit test.

Specialties & Licenses

★ Primary SpecialtyClinical Medical LaboratoryLaboratories

Taxonomy Code291U00000X

Licenses✔ Licensed in NJ · 00007503✔ Licensed in NJ · 25MA05880800

Definition

(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.

25 RIVERSIDE DR STE 2, Pine Brook, NJ 07058

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Other Identifiers 12

OtherP00213695Railroad

OtherSI0S64U020Empire Bcbs

Other000000039833Boston Medical Center

Other269580Amerigroup

Other250588080Hipusa

Other7262661Aetna

Medicaid0066222NJ

Other427253Tufts Health Plan

Other60013223Horizon Nj Health

Other9759537Ghi

OtherA3638184Oxford Health Plan

OtherJ35526Healthnet

Accepted Insurance

The full list of accepted plans is on the Insurance tab. Issuers include Blue Cross Blue Shield of Arizona.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.

Certificate of Accreditation 31D1028659

Si Paradigm LLC · Pine Brook, NJ

Active · expires Mar 20, 2027

CLIA Number31D1028659

Laboratory TypeIndependent

Certificate Effective DateMarch 21, 2025

Certificate Expiration DateMarch 20, 2027

Laboratory DirectorDr. Sherif A. Nasr

Laboratory Phone(201) 599-9044

Laboratory LocationSi Paradigm LLC25 Riverside Drive Suite 2, Pine Brook, NJ 07058

CLIA data matches this NPI record on: Address 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 claims 64

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.

Flow cytometry technique for dna or cell analysis, each additional marker 88185

Flow cytometry is a technique that helps analyze the physical and chemical characteristics of cells or particles. When an additional marker is used, it aids in identifying specific cell types or stages of disease. This helps in precise diagnosis and treatment planning.

41,095 services1,698 patients

Microscopic genetic analysis of tissue, manual, each additional multiplex stain procedure 88377

Microscopic genetic analysis of tissue is a detailed lab process that examines your cells' genetic material. If more than one stain procedure is needed, it's termed an 'additional multiplex stain procedure'. This helps to highlight different components within your cells, aiding in accurate diagnosis and treatment planning.

4,635 services1,347 patients

Special stained specimen slides to examine tissue, each additional procedure 88341

Special stained specimen slides are used to analyze tissue in detail. In this process, extra procedures may be needed for a more thorough examination. These involve applying special stains to the tissue on slides, enhancing specific elements for closer study.

3,836 services717 patients

Molecular pathology procedure; physician interpretation and report G0452

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.

3,447 services3,025 patients

Special stained specimen slides to examine tissue including interpretation and report 88313

Special stained specimen slides are used to examine tissue samples. This involves applying special dyes to the tissue, which helps to highlight certain features under a microscope. The findings are then interpreted and a report is provided. This can aid in diagnosing various health conditions.

2,527 services580 patients

Flow cytometry technique for dna or cell analysis, 16 or more markers 88189

Flow cytometry is a method used to measure and analyze cells. It uses a beam of light to detect up to 16 or more markers on cells, helping to identify their type, function, or abnormalities. This technique aids in diagnosing various health conditions.

2,041 services1,875 patients

Microscopic genetic analysis of tissue, manual, each additional multiplex stain procedure 88377

1,909 services571 patients

Flow cytometry technique for dna or cell analysis, first marker 88184

Flow cytometry is a technique used to examine microscopic particles, like cells or DNA. It employs a beam of light to detect and measure physical and chemical characteristics of these particles. The 'first marker' refers to a specific characteristic or feature used to identify a particular cell or particle.

1,824 services1,703 patients

Special stained specimen slides to examine tissue, each additional procedure 88341

1,757 services314 patients

Genomic sequence analysis panel of dna or combined dna and rna of 51 or more genes associated with blood and lymphatic system disorders 81455

A genetic test for cancer is a medical test that checks your DNA for changes or mutations that might put you at risk for cancer. It's a proactive step to understand your health better and possibly take preventive measures if needed.

1,302 services1,236 patients

Special stained specimen slides to examine tissue including interpretation and report 88313

1,087 services255 patients

Pathology examination of tissue using a microscope, intermediate complexity 88305

A pathology examination of tissue with intermediate complexity involves studying a small sample of your body tissue under a microscope. This helps in identifying any abnormal cells or signs of disease. It's a detailed process requiring expert analysis to ensure accurate results.

1,010 services595 patients

Tissue culture for tumor disorders of bone marrow and blood cells 88237

Tissue culture for tumor disorders of bone marrow and blood cells is a lab process where your cells are grown in a controlled environment. The aim is to detect and study abnormal cells, such as cancer, in your bone marrow or blood. This helps in planning effective treatment.

796 services773 patients

Special stained specimen slides to examine tissue, initial procedure 88342

This procedure involves the use of specially stained slides to examine tissue samples. The initial process involves obtaining a small tissue sample from your body. This sample is then placed on a slide and stained with special dyes to highlight different structures and elements. The stained slide is then examined under a microscope to help diagnose any potential health issues.

770 services740 patients

Interpretation and report of genetic testing 88291

Interpretation and report of genetic testing involves analyzing your DNA to look for changes that could indicate a risk for certain health conditions. The results are then compiled into a report, which provides insights about your genetic health.

768 services746 patients

Flow cytometry technique for dna or cell analysis, 16 or more markers 88189

759 services721 patients

Chromosome analysis for genetic defects, analyze 20-25 cells 88264

Chromosome analysis is a test that evaluates your cells to check for genetic defects. In this procedure, 20-25 cells are examined under a microscope to identify any abnormalities. This information can help in diagnosing certain genetic conditions and guide treatment plans.

745 services725 patients

Microscopic genetic analysis of tissue, manual, initial procedure 88368

Microscopic genetic analysis of tissue is a test that examines your cells under a microscope. This helps to identify any genetic changes that could be causing health issues. It's the first step in a series of tests to pinpoint the root cause of your symptoms.

696 services680 patients

Bone marrow, smear interpretation 85097

Bone marrow smear interpretation is a procedure where a small sample of your bone marrow is taken and examined under a microscope. This helps doctors identify any abnormal cells or signs of diseases such as anemia, leukemia, or infections. It's a crucial step in diagnosing various blood disorders.

593 services574 patients

Preparation of tissue for examination by removing any calcium present 88311

This procedure involves treating tissue samples to remove any calcium, which can interfere with the examination. The tissue is soaked in a special solution that safely dissolves the calcium, leaving the tissue intact for accurate analysis. This helps in making precise diagnoses.

589 services572 patients

Pathology examination of tissue using a microscope, intermediate complexity 88305

463 services256 patients

Translocation analysis (bcr/abl1) major breakpoint 81206

Translocation analysis (bcr/abl1) major breakpoint is a test that checks for a specific gene rearrangement in your cells. This rearrangement is often seen in certain types of leukemia. The test helps doctors diagnose and monitor treatment for these conditions.

386 services178 patients

Cell examination of specimen, selective cellular enhancement technique 88112

Cell examination of a specimen using selective cellular enhancement technique is a lab process that improves the visibility of certain cells in a sample. It helps in identifying abnormalities or diseases. The process is non-invasive, safe, and aids in accurate diagnosis.

374 services361 patients

Special stained specimen slides to examine tissue, initial procedure 88342

344 services334 patients

Preparation of specimen, manual 88381

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.

322 services320 patients

Microscopic genetic analysis of tumor, manual 88360

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.

310 services273 patients

Microscopic genetic analysis of tissue, manual, initial procedure 88368

310 services303 patients

Interpretation and report of genetic testing 88291

294 services287 patients

Complete blood cell count (red cells, white blood cell, platelets), automated test and automated differential white blood cell count 85025

A Complete Blood Cell Count is a common test that measures various components of the blood, including red cells (carry oxygen), white cells (fight infection), and platelets (help blood clot). An automated test ensures accuracy. The differential count provides detailed information about white cell types.

289 services274 patients

Bone marrow, smear interpretation 85097

263 services258 patients

Preparation of tissue for examination by removing any calcium present 88311

254 services249 patients

Genomic sequence analysis panel of dna or combined dna and rna of 5-50 genes associated with blood and lymphatic system disorders 81450

This test examines your DNA to identify any genetic changes that could indicate a risk for blood-related cancers. It's a simple process where a sample of your blood or saliva is taken and sent to a lab for detailed examination.

233 services225 patients

Gene analysis (janus kinase 2) targeted sequence analysis 81279

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.

232 services227 patients

Gene rearrangement analysis (immunoglobulin heavy chain locus), variable region somatic mutation analysis 81263

Gene rearrangement analysis is a test that studies alterations in your immune system's DNA. Specifically, it evaluates the variable region somatic mutation in the immunoglobulin heavy chain locus, which helps understand your body's immune response.

205 services202 patients

Genomic sequence analysis panel of dna or combined dna and rna of 5-50 genes associated with solid organ abnormal growth of tissue 81445

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.

186 services186 patients

Cell examination of specimen, selective cellular enhancement technique 88112

170 services167 patients

Flow cytometry technique for dna or cell analysis, 9 to 15 markers 88188

Flow cytometry is a technique used to measure physical and chemical characteristics of cells or particles. It can analyze multiple markers (9 to 15) on a cell, helping to identify its type and function. This process can also examine DNA within cells for any abnormalities.

170 services167 patients

Gene analysis (mpl proto-oncogene, thrombopoietin receptor) for detection of common variants 81338

Gene analysis for the MPL proto-oncogene, thrombopoietin receptor, is a test that looks for common genetic variants. This helps in understanding certain health conditions related to blood cell production. It's a non-invasive procedure, involving a simple blood draw.

155 services152 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.

145 services143 patients

Translocation analysis (bcr/abl1) minor breakpoint 81207

Translocation analysis (bcr/abl1) minor breakpoint is a genetic test that identifies specific changes in chromosomes. It's used to diagnose certain types of blood cancers. The test detects rearrangements of genetic material, aiding in the treatment plan.

134 services68 patients

Preparation of specimen, manual 88381

95 services94 patients

Microscopic genetic analysis of tumor, manual 88360

83 services78 patients

Microscopic genetic analysis of tissue, manual, each additional procedure 88369

Microscopic genetic analysis of tissue is a procedure where a small sample of your body tissue is examined under a microscope. This is done to study the genes in your cells. If more than one procedure is needed, each additional one involves repeating this process. It's a key part of diagnosing and managing many health conditions.

54 services51 patients

Gene analysis (breast cancer 1 and 2) of full sequence and analysis for duplication or deletion variants 81162

Gene analysis for breast cancer 1 and 2 involves studying your DNA to detect alterations that may increase your risk of developing certain health issues. This test analyzes the full sequence and checks for duplication or deletion variants.

49 services49 patients

Gene analysis (myeloid differentiation primary response 88) for p.leu265pro variant 81305

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.

45 services45 patients

Gene analysis (calreticulin), common variants 81219

Gene analysis of calreticulin, common variants, is a test that looks at specific genes to identify changes that may cause certain health issues. It helps in understanding your genetic makeup and potential health risks. It's a simple procedure involving a blood or saliva sample.

42 services42 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.

40 services40 patients

Flow cytometry technique for dna or cell analysis, 9 to 15 markers 88188

38 services37 patients

Genetic sequencing localization, initial procedure 88365

Genetic sequencing localization is a process to identify where specific genes are located in your DNA. During the initial procedure, a sample of your cells is collected, usually through a simple swab or blood test. This data is then analyzed to pinpoint the location of certain genes. This can help understand your genetic makeup and potential health risks.

33 services29 patients

Gene analysis (v-raf murine sarcoma viral oncogene homolog b1) 81210

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.

32 services31 patients

Genetic sequencing localization, each additional procedure 88364

Genetic sequencing localization is a process where specific regions of your DNA are identified and studied. If you're having additional procedures, it simply means that more areas of your DNA are being examined. This helps to understand your genetic makeup better and can assist in identifying potential health risks.

28 services17 patients

Genetic sequencing localization, initial procedure 88365

27 services27 patients

Chromosome analysis for genetic defects, additional karyotypes, each study 88280

Chromosome analysis is a test that examines the number and structure of a person's chromosomes. This is done to identify any genetic defects. Additional karyotypes, each study, are further tests that look at the arrangement of these chromosomes. This can help in detecting genetic disorders.

25 services25 patients

Genetic sequencing localization, each additional procedure 88364

25 services20 patients

Gene analysis (abl proto-oncogene 1, non-receptor tyrosine kinase) 81170

Gene analysis of the ABL1 gene helps identify changes that may cause certain health issues. It involves examining the ABL1 gene, which makes a protein involved in cell division and communication. This test aids in diagnosing and managing treatment for these conditions.

24 services17 patients

Chromosome analysis for genetic defects, count 5 cells 88261

Chromosome analysis is a test that examines the number and structure of your cells. It helps identify any genetic defects that might cause health issues. In this procedure, 5 cells are analyzed to ensure accuracy. The results may provide crucial information for your health management.

19 services19 patients

Gene analysis (muts homolog 6 [e coli]) full sequence analysis 81298

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.

17 services17 patients

Gene analysis (postmeiotic segregation increased 2 [s cerevisiae]) full sequence analysis 81317

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.

17 services17 patients

Surgical pathology consultation and report on referred slides prepared elsewhere 88321

A surgical pathology consultation involves reviewing slides prepared at a different lab to confirm or clarify a diagnosis. It's a second opinion to ensure accuracy. A report with findings and interpretations is then provided for your doctor's reference.

17 services17 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.

16 services16 patients

Flow cytometry technique for dna or cell analysis, 2 to 8 markers 88187

Flow cytometry is a technique that helps analyze your cells and DNA. It uses lasers to identify and sort cells based on their properties, marked by up to 8 different markers. This helps in diagnosing and monitoring various health conditions.

16 services15 patients

Chromosome analysis for genetic defects, additional cells counted, each study 88285

Chromosome analysis is a study that examines your body's chromosomes to identify any genetic defects. In some cases, additional cells may be counted to ensure accuracy. This can provide valuable information about potential health risks and inform treatment decisions.

16 services16 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.

15 services15 patients

Microscopic genetic analysis of tissue, manual, each additional procedure 88369

14 services12 patients

Other Providers at the Same Location NPPES 5

Providers registered at the same practice address, or within the immediate area, according to the NPPES registry.

MR. SAUD SAQIB RAHMAN MD

Pathology (Anatomic Pathology & Clinical Pathology)