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MERIDIAN BIOSCIENCE

MERIDIAN BIOSCIENCE

Meridian Bioscience manufactures, markets, and distributes diagnostic test kits, purified reagents and biopharmaceutical-enabling technologies for the early diagnosis and treatment of common medical conditions. Its products are ideal for hospitals, reference laboratories, research centers, physician offices and diagnostic ...
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Covid-19 MERIDIAN BIOSCIENCE

Clinical Laboratory

SARS-CoV-2 rRT-PCR Test
Revogene SARS-CoV-2

Revogene SARS-CoV-2 is a real-time Reverse Transcription Polymerase Chain Reaction (rRT-PCR) qualitative test run on the Revogene instrument for the detection of SARS-CoV-2 nucleic acid from nasopharyngeal, oropharyngeal, anterior nasal, and mid-turbinate nasal swab specimens. The test can return a positive result as soon as 47 minutes and provides impressive clinical performance with a positive predictive agreement (PPA) of 97.7% and a negative predicative agreement (NPA) of 97.7%.
More details

SARS-CoV-2 Antigen Test
GenBody COVID-19 Ag

GenBody COVID-19 Ag is an immunochromatographic assay kit for the qualitative detection of SARS-CoV-2 antigen in a nasopharyngeal swab from humans. The lateral flow immunoassay offers detection of active infection caused by SARS-CoV-2 in 15 minutes and allows for near patient testing without the need of instrumentation or special equipment.
More details

COVID-19 IgG/IgM Test
QuikPac II 2019 COVID-19

The QuikPac II 2019 COVID-19 IgG and IgM Test is a qualitative test for the detection of IgG and IgM antibodies to COVID-19 in human serum, plasma or whole blood. The test provides a differential detection of anti-SARS-CoV-2 IgM and anti-SARS-CoV-IgG antibodies and can be used for the presumptive distinction between a primary and secondary Coronavirus infection.
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Molecular Diagnostic Instrument
Revogene

Revogene is a flexible molecular platform capable of single analyte and multiplex testing that is packaged in a small footprint, and can help standardize testing throughout the health system. The fully automated molecular platform offers minimal hands-on time with walk-away efficiencies.
More details

Molecular Reagents
Molecular Reagents

Meridian’s portfolio of RT-qPCR master mixes have been designed to simplify the development of SARS-CoV-2 molecular assays and enable new features such as extraction-free amplification. Each master mix contains a hot-start polymerase, dNTPs, buffer and other components optimized for each particular application (e.g. lyophilization). Only primers and probes are required to complete the assay formula. Meridian has developed an Inhibitor-Tolerant RT-qPCR Mix capable of delivering sensitive multiplex detection, even in the presence of difficult inhibitors found in sputum, saliva and stool specimens. This new mix offers a novel alternative to nucleic acids extraction, saving both time and labor which are vitally important in viral screening assays that require rapid detection for infection control.
More details

SARS-CoV-2 High Sensitivity Antibodies
SARS-CoV-2 High Sensitivity Antibodies

Meridian’s monoclonal antibodies are highly sensitive for the detection of SARS-CoV-2 and they do not cross-react with seasonal coronavirus strains. They are ideal for developing reliable and sensitive rapid lateral flow antigen assays for the detection of active COVID-19 infections.
More details

SARS-CoV-2 Recombinant Antigens
SARS-CoV-2 Recombinant Antigens

Meridian’s recombinant antigens are expressed in human mammalian cells and insect cells using proprietary expression and purification technologies. Expression in either human or insect cells provides for post-translational modifications such as glycosylation and phosphorylation which can offer significant performance advantages over E. coli expressed formats.
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News of MERIDIAN BIOSCIENCE

Meridian Bioscience Acquired by SD Biosensor and SJL Partners

08 Jul 2022
Meridian Bioscience Acquired by SD Biosensor and SJL Partners
Meridian Bioscience, Inc. (Cincinnati, OH, USA) and SD Biosensor, Inc. (Seoul, South Korea) and SJL Partners LLC (Seoul, South Korea) have entered into a definitive merger agreement whereby a newly formed affiliate vehicle of the consortium will acquire Meridian in an all-cash transaction valued at approximately USD 1.53 billion.
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Meridian Acquires Euprotein to Further Expand Recombinant Protein Capabilities

03 May 2022
Meridian Acquires Euprotein to Further Expand Recombinant Protein Capabilities
Meridian Bioscience, Inc. (Cincinnati, OH, USA) has acquired, through its subsidiary Meridian Life Science, Inc., substantially all of the assets of EUPROTEIN Inc. (North Brunswick Township, NJ, USA).
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About MERIDIAN BIOSCIENCE

Meridian Bioscience manufactures, markets, and distributes diagnostic test kits, purified reagents and biopharmaceutical-enabling technologies for the early diagnosis and treatment of common medical conditions. Its products are ideal for hospitals, reference laboratories, research centers, physician offices and diagnostics manufacturers.

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Bordetella Pertussis Molecular Assay
Alethia Pertussis

The Alethia Pertussis assay is designed for the detection of Bordetella pertussis, the bacterium responsible for whooping cough. Employing LAMP technology, it offers high sensitivity and specificity, providing reliable results for effective patient management. The assay's efficient design reduces the potential for cross-contamination and ensures consistent performance across various sample types.
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Group A Streptococcus Molecular Test
Alethia Group A Streptococcus

The Alethia Group A Streptococcus assay is a molecular test developed for the precise detection of Streptococcus pyogenes, the bacterium responsible for strep throat and other infections. Utilizing loop-mediated isothermal amplification (LAMP) technology, this assay delivers rapid and accurate results, facilitating timely diagnosis and treatment. Its streamlined workflow and minimal hands-on time make it suitable for various laboratory settings, enhancing efficiency in clinical diagnostics.
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Herpes Simplex Virus 1&2 Assay
Alethia HSV 1&2

The Alethia HSV 1&2 assay is designed for the detection and differentiation of Herpes Simplex Virus types 1 and 2. Employing LAMP technology, it offers high sensitivity and specificity, providing reliable results for effective patient management. The assay's efficient design reduces the potential for cross-contamination and ensures consistent performance across various sample types.
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Clinical Laboratory

Bordetella Pertussis Molecular Assay
Alethia Pertussis

The Alethia Pertussis assay is designed for the detection of Bordetella pertussis, the bacterium responsible for whooping cough. Employing LAMP technology, it offers high sensitivity and specificity, providing reliable results for effective patient management. The assay's efficient design reduces the potential for cross-contamination and ensures consistent performance across various sample types.
More details

Group A Streptococcus Molecular Test
Alethia Group A Streptococcus

The Alethia Group A Streptococcus assay is a molecular test developed for the precise detection of Streptococcus pyogenes, the bacterium responsible for strep throat and other infections. Utilizing loop-mediated isothermal amplification (LAMP) technology, this assay delivers rapid and accurate results, facilitating timely diagnosis and treatment. Its streamlined workflow and minimal hands-on time make it suitable for various laboratory settings, enhancing efficiency in clinical diagnostics.
More details

Herpes Simplex Virus 1&2 Assay
Alethia HSV 1&2

The Alethia HSV 1&2 assay is designed for the detection and differentiation of Herpes Simplex Virus types 1 and 2. Employing LAMP technology, it offers high sensitivity and specificity, providing reliable results for effective patient management. The assay's efficient design reduces the potential for cross-contamination and ensures consistent performance across various sample types.
More details

Neisseria Gonorrhea Molecular Test
Alethia Gonorrhea

The Alethia Gonorrhea assay is a molecular test developed for the precise detection of Neisseria gonorrhoeae. Utilizing loop-mediated isothermal amplification (LAMP) technology, this assay delivers rapid and accurate results, facilitating timely diagnosis and treatment. Its streamlined workflow and minimal hands-on time make it suitable for various laboratory settings, enhancing efficiency in clinical diagnostics.
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Cytomegalovirus Assay
Alethia CMV

Alethia CMV is a molecular diagnostic assay designed for the qualitative detection of Cytomegalovirus (CMV) DNA. Utilizing loop-mediated isothermal amplification (LAMP) technology, it offers rapid and accurate results, aiding in the timely diagnosis of CMV infections. The assay is user-friendly and integrates seamlessly into laboratory workflows.
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Chlamydia Trachomatis Assay
Alethia Chlamydia

Alethia Chlamydia is a molecular assay intended for the qualitative detection of Chlamydia trachomatis DNA. Employing LAMP technology, it provides rapid and reliable results, facilitating the diagnosis of chlamydial infections. The assay is designed for ease of use and fits well into existing laboratory procedures.
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Malaria Test
Alethia Malaria

Alethia Malaria is a molecular diagnostic test for the qualitative detection of Plasmodium species DNA, the causative agents of malaria. Utilizing LAMP technology, it delivers rapid and accurate results, essential for the timely diagnosis and treatment of malaria. The assay is user-friendly and compatible with standard laboratory workflows.
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Helicobacter Pylori Test
Curian HpSA

The Curian HpSA is a rapid, qualitative immunoassay designed for the detection of Helicobacter pylori antigens in human stool samples. Utilizing advanced immunochromatographic technology, it provides accurate results to aid in the diagnosis of H. pylori infections and to confirm eradication post-treatment. The assay is user-friendly, delivering results efficiently, making it suitable for both clinical laboratories and point-of-care settings.
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Coccidioidomycosis Test
Premier Coccidioides Antibody Test

The Premier Coccidioides Antibody Test is a serological assay for diagnosing coccidioidomycosis. With enhanced sensitivity and specificity, it enables the detection of IgG and IgM antibodies in serum. This test aids in the early diagnosis of fungal infections, supporting targeted treatment and improved patient outcomes.
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Varicella-Zoster Virus Test
Merifluor VZV Kit

The Merifluor VZV Kit uses advanced immunofluorescence technology for the detection of varicella-zoster virus in clinical specimens. It provides fast and precise results, making it an essential tool for diagnosing viral infections. Its high accuracy and ease of use support laboratory efficiency and reliable patient care.
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Cryptosporidium/Giardia Test
Merifluor Cryptosporidium/Giardia Kit

The Merifluor Cryptosporidium/Giardia Kit is a fluorescence-based diagnostic tool for detecting Cryptosporidium and Giardia in clinical specimens. It offers high sensitivity and specificity, ensuring rapid and accurate results. This kit is ideal for gastrointestinal disease diagnostics in laboratories seeking reliable parasite identification.
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Respiratory Syncytial Virus Test
TRU RSV Diagnostic Kit

The TRU RSV Diagnostic Kit offers rapid and accurate detection of respiratory syncytial virus (RSV). Using lateral flow immunoassay technology, it delivers results in under 15 minutes. Its easy-to-use format is designed for point-of-care settings, providing reliable diagnostics that aid in timely clinical decision-making for respiratory illnesses.
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Clostridium Difficile Assay
Revogene C. Difficile

The Revogene C. difficile assay is a qualitative in vitro diagnostic test that utilizes automated sample processing and real-time polymerase chain reaction (PCR) to detect the toxin B (tcdB) gene of toxigenic Clostridium difficile (C. difficile) in unformed (liquid or soft) stool specimens obtained from patients suspected of having C. difficile infection (CDI). The Revogene C. difficle assay is performed on the Revogene instrument and is intended to aid in the diagnosis of CDI.
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Carbapenem-Resistant Enterobacterales Assay
Revogene Carba C

The Revogene Carba C assay enables early detection and management of Carbapenem-Resistant Enterobacterales (CRE) from isolated colonies of Enterobacteriaceae, Acinetobacter baumannii, or Pseudomonas aeruginosa. The assay is intended as an aid for infection control in the detection of carbapenem-non- susceptible bacteria that colonize patients in healthcare settings.
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Clostridium Difficile Toxin A & B Test
Premier Toxins A&B

Premier Toxins A&B is a qualitative enzyme immunoassay for the detection of Clostridium difficile toxin A and toxin B in stool from patients with antibiotic-associated diarrhea. It is intended for use as an aid in the diagnosis of C. difficile-associated disease (CDAD).
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Clostridium Difficile Test
Premier C. difficile GDH

Premier C. difficile GDH is a qualitative enzyme immunoassay screening test for the direct detection of Clostridium difficile antigen, glutamate dehydrogenase, in fecal samples from symptomatic persons suspected of having C. difficile infection (CDI). This test does not distinguish between toxigenic and non-toxigenic strains of C. difficile.
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Blood Lead Testing Solution
LeadCare Ultra

LeadCare Ultra is the first plug-and-play, benchtop solution for blood lead testing, offering users calibration at the touch of a button and results in 3 minutes. It is based on anodic stripping voltammetry (ASV), an electrochemical technique that has been used in clinical laboratories for decades, and offers throughput and convenience for high-volume labs.
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Blood Lead Test Kit
LeadCare Plus

LeadCare Plus is a stand-alone, single-channel analyzer based on anodic stripping voltammetry (ASV) for labs with lower sample volumes. The plug-in-and-go analyzer without any setup or maintenance costs features a data management system that offers easy integration with a laboratory’s LIS (optional).
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Mononucleosis Agglutination Test
MONOSPOT Latex

MONOSPOT Latex is a one step rapid latex particle agglutination test for the qualitative and semiquantitative determination of infectious mononucleosis heterophile antibodies in serum or plasma. The test is intended to aid in the diagnosis of infectious mononucleosis.
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Campylobacter Antigen Test
Immunocard STAT! CAMPY

Immunocard STAT! CAMPY is a one-step lateral flow immunoassay for the direct detection of Campylobacter antigen from stool specimens. It delivers results in 20 minutes and allows for the triage of patients for earlier therapy.
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E. coli Test
Immunocard STAT E. coli O157 Plus

Immunocard STAT E. coli O157 Plus is a one-step lateral flow immunoassay for the direct detection of Shiga Toxin-Producing E. coli O157 in stool specimens and culture. It provides direct qualitative results within 10 minutes that are interpreted visually by the presence or absence of a colored line.
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Influenza A and B Test
Immunocard STAT! Flu A&B

The Immunocard STAT! Flu A&B is an in vitro rapid qualitative test that detects influenza type A and type B nucleoprotein antigens directly from nasal swabs, nasopharyngeal swabs, and nasopharyngeal aspirate/wash specimens obtained from patients with signs and symptoms of respiratory infection. It is intended to aid in the rapid differential diagnosis of influenza A and B viral infections.
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Human Chorionic Gonadotropin Test
Immunocard STAT hCG

Immunocard STAT hCG is a CLIA-waived one-step lateral flow immunoassay for the direct detection of human chorionic gonadotropin (hCG) in urine and serum samples. It provides simple, easy-to-read results in three minutes for urine and five minutes for serum, making it ideal for use as an aid in the early determination of pregnancy.
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Streptococcus B Test
Alethia Group B Streptococcus Assay

The Alethia Group B Streptococcus assay is a qualitative in vitro diagnostic for the detection of Streptococcus agalactiae in enriched cultures obtained from vaginal/rectal swab specimens from antepartum women. The test’s molecular precision ensures accurate results and timely administration of appropriate antibiotic therapy for GBS-positive patients.
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Streptococcus A Test
Revogene Strep A Assay

The Revogene Strep A assay is for the direct detection of Streptococcus pyogenes (Group A β-hemolytic Streptococcus; GAS) from throat swab specimens obtained from patients with signs and symptoms of pharyngitis. This test can provide final results in as early as 42 minutes for positive specimens.
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C. difficile Test
Alethia C.difficile Assay

The Alethia C.difficile assay is a quick, accurate and reliable molecular assay for C. difficile detection. By providing accurate and reliable results, the assay allows for appropriate management and treatment of their patients.
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Group B Streptococcus Test
Revogene GBS LB Assay

The Revogene GBS LB assay is a qualitative in vitro diagnostic test to detect Group B Streptococcus (GBS) from vaginal/rectal swab samples, after Lim Broth enrichment, from antepartum pregnant women. The assay provides physicians with accurate and reliable results within 70 minutes, allowing for appropriate treatment decisions of the mother at the time of delivery, ensuring the best outcome for the baby.
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POC Blood Lead Poisoning Test
LeadCare II

LeadCare II is the only CLIA waived point-of-care test for blood lead poisoning and can screen in a single visit with a simple finger-stick in just three minutes. The system includes the LeadCare II Blood Lead Analyzer and the LeadCare II Test Kit and is designed for the quantitative measurement of lead in fresh whole blood.
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Pneumocystis Test
MERIFLUOR

MERIFLUOR Pneumocystis is an in vitro procedure for the detection of Pneumocystis carinii cysts and trophozoites in direct smears of respiratory tract specimens. It provides a simple, highly specific, direct immunofluorescent procedure for the identification of P. carinii cysts and trophozoites in respiratory tract specimens.
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Legionella Rapid Antigen Test
TRU Legionella

TRU Legionella is a Rapid Immunoassay for the detection of Legionella pneumophila serogroup 1 antigens in human urine specimens. It improves lab efficiency with a simple, 3-step procedure and enables physicians to make informed decisions about the management and treatment of their patients.
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Automated CLIA Analyzer
LIAISON XL

The LIAISON XL is a fully automated chemiluminescence (CLIA) analyzer that performs complete sample processing using “Flash” CLIA technology with paramagnetic microparticle solid phase. It performs complete sample processing (sample pre-dilutions, sample and reagent dispensing, incubations, wash processes, etc.) as well as measurement and evaluation.
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Urea Breath Test System
BreathID Hp

The BreathID Hp urea breath test system for H. pylori detection intuitively combines market-leading diagnostic accuracy with real-time results and convenient follow-up testing in a clinic or point-of-care setting. It offers market-leading performance and compact efficiencies with its real-time results enabling providers to test and treat at the point of care.
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SARS-CoV-2 rRT-PCR Test
Revogene SARS-CoV-2

Revogene SARS-CoV-2 is a real-time Reverse Transcription Polymerase Chain Reaction (rRT-PCR) qualitative test run on the Revogene instrument for the detection of SARS-CoV-2 nucleic acid from nasopharyngeal, oropharyngeal, anterior nasal, and mid-turbinate nasal swab specimens. The test can return a positive result as soon as 47 minutes and provides impressive clinical performance with a positive predictive agreement (PPA) of 97.7% and a negative predicative agreement (NPA) of 97.7%.
More details

Campylobacter Enzyme Immunoassay
Premier CAMPY

The Premier CAMPY is an enzyme immunoassay that detects Campylobacter antigens and is intended for testing of stool samples from patients with signs and symptoms of gastroenteritis. The highly sensitive assay provides detection without lengthy and variable culture procedures and has a faster turnaround time of two hours.
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Urea Breath Test System
BreathID Smart

The state-of-the-art BreathID Smart urea breath test system for H. pylori detection intuitively combines market-leading diagnostic accuracy with efficient automation, all in a compact footprint for maximizing mid-range testing throughput. The BreathID platform can be used in conjunction with other Meridian H. pylori platforms for a total testing solution across the healthcare system.
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Blood Lead Test Analyzer
LeadCare

LeadCare is a blood lead test platform that provides a stand-alone system and features the only CLIA waived system to help core labs, hospital labs, reference labs, or physician’s office labs run more efficiently. It provides accurate, three-minute quantitative blood lead results, allowing physicians to educate and take action immediately.
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Helicobacter Pylori IgG Assay
Premier H. pylori

Premier H. pylori is a streamlined, highly sensitive enzyme immunoassay for the in vitro qualitative detection of IgG antibodies to Helicobacter pylori in human serum and plasma. The test results are intended to aid in the diagnosis of H. pylori infection.
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Urea Breath Test System for H. Pylori
BreathID Hp Lab

The BreathID Hp Lab is a state-of-the-art urea breath test system for H. pylori detection that intuitively combines market-leading diagnostic accuracy with efficient automation and fast batch-test analysis for maximizing large lab testing throughput. It offers a user-friendly interface and a cost-effective clinical diagnostic solution that can be used in any clinical setting, including office-based practices, hospitals, laboratories and the ICU.
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Fluorescence Immunoassay Analyzer
Curian

Curian is an efficient fluorescence immunoassay platform focused in gastrointestinal testing that is packaged in a small footprint to improve hospital operational efficiencies. Curian provides healthcare systems a rapid fluorescence immunoassay diagnostic solution with a standardized, simplified workflow that eliminates subjectivity. Laboratories can eliminate workflow burdens and achieve optimal efficiency while delivering top-of-the-line patient care.
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LAMP Molecular Diagnostic System
Alethia

The Alethia is an affordable LAMP (loop-mediated isothermal amplification) based molecular platform with a simple to use instrument that generates between 1 - 10 qualitative results in less than one hour. The molecular platform addresses your lab’s broad-spectrum needs, simply and accurately, with results that enable evidence-based health decisions.
More details

SARS-CoV-2 Recombinant Antigens
SARS-CoV-2 Recombinant Antigens

Meridian’s recombinant antigens are expressed in human mammalian cells and insect cells using proprietary expression and purification technologies. Expression in either human or insect cells provides for post-translational modifications such as glycosylation and phosphorylation which can offer significant performance advantages over E. coli expressed formats.
More details

SARS-CoV-2 High Sensitivity Antibodies
SARS-CoV-2 High Sensitivity Antibodies

Meridian’s monoclonal antibodies are highly sensitive for the detection of SARS-CoV-2 and they do not cross-react with seasonal coronavirus strains. They are ideal for developing reliable and sensitive rapid lateral flow antigen assays for the detection of active COVID-19 infections.
More details

Molecular Reagents
Molecular Reagents

Meridian’s portfolio of RT-qPCR master mixes have been designed to simplify the development of SARS-CoV-2 molecular assays and enable new features such as extraction-free amplification. Each master mix contains a hot-start polymerase, dNTPs, buffer and other components optimized for each particular application (e.g. lyophilization). Only primers and probes are required to complete the assay formula. Meridian has developed an Inhibitor-Tolerant RT-qPCR Mix capable of delivering sensitive multiplex detection, even in the presence of difficult inhibitors found in sputum, saliva and stool specimens. This new mix offers a novel alternative to nucleic acids extraction, saving both time and labor which are vitally important in viral screening assays that require rapid detection for infection control.
More details

Molecular Diagnostic Instrument
Revogene

Revogene is a flexible molecular platform capable of single analyte and multiplex testing that is packaged in a small footprint, and can help standardize testing throughout the health system. The fully automated molecular platform offers minimal hands-on time with walk-away efficiencies.
More details

COVID-19 IgG/IgM Test
QuikPac II 2019 COVID-19

The QuikPac II 2019 COVID-19 IgG and IgM Test is a qualitative test for the detection of IgG and IgM antibodies to COVID-19 in human serum, plasma or whole blood. The test provides a differential detection of anti-SARS-CoV-2 IgM and anti-SARS-CoV-IgG antibodies and can be used for the presumptive distinction between a primary and secondary Coronavirus infection.
More details

SARS-CoV-2 Antigen Test
GenBody COVID-19 Ag

GenBody COVID-19 Ag is an immunochromatographic assay kit for the qualitative detection of SARS-CoV-2 antigen in a nasopharyngeal swab from humans. The lateral flow immunoassay offers detection of active infection caused by SARS-CoV-2 in 15 minutes and allows for near patient testing without the need of instrumentation or special equipment.
More details

Immunoassay Test
TRU FLU

The TRU FLU is a rapid, 15-minute assay for the detection and differentiation of influenza A and influenza B. The closed system limits exposure to influenza during test incubation and disposal, and offers superior performance on flu A, which has much higher prevalence and virulence than flu B.
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Immunoassay Test
ImmunoCard STAT! Strep A

The ImmunoCard STAT! Strep A is a rapid immunoassay for the detection of Group A Streptococcal antigen. It has a shelf life of 10 months and can be stored in room temperature.
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Immunoassay Test
ImmunoCard Mycoplasma

The ImmunoCard Mycoplasma is the only rapid EIA for the detection of IgM to Mycoplasma pneumoniae in human serum. It offers a simple four-step procedure for the detection of active Mycoplasma pneumoniae infection in just nine minutes.
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Incubator/Reader
illumipro-10

The illumipro-10 is an automated isothermal amplification and detection system that combines Loop-Mediated Isothermal Amplification (LAMP) technology with a very simple assay process. It provides continuous access while running up to 10 samples at a time in two independent five-sample chambers and displays the results directly on a LED readout screen.
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HpSA Immuonoassay
ImmunoCard STAT HpSA

The ImmunoCard STAT HpSA is a rapid one-step immunoassay for the detection of H. pylori antigens in human stool that can be used to diagnose, monitor and confirm eradication. The monoclonal antibody-based test can provide accurate results in five minutes and has a shelf life of 24 months from the date of manufacture.
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Point-Of-Care Testing

Respiratory Syncytial Virus Test
TRU RSV Diagnostic Kit

The TRU RSV Diagnostic Kit offers rapid and accurate detection of respiratory syncytial virus (RSV). Using lateral flow immunoassay technology, it delivers results in under 15 minutes. Its easy-to-use format is designed for point-of-care settings, providing reliable diagnostics that aid in timely clinical decision-making for respiratory illnesses.
More details

POC Blood Lead Poisoning Test
LeadCare II

LeadCare II is the only CLIA waived point-of-care test for blood lead poisoning and can screen in a single visit with a simple finger-stick in just three minutes. The system includes the LeadCare II Blood Lead Analyzer and the LeadCare II Test Kit and is designed for the quantitative measurement of lead in fresh whole blood.
More details
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