VereBeef™ Detection Kit is a multiplex test combining both Polymerase Chain Reaction (PCR) and microarray technologies into a single testing workflow. This product is intended for qualitative detection, differentiation and identification of multiple food-borne pathogens in raw beef trim and is certified for use by the Association of Official Analytical Chemists (AOAC Research Institute) in the US.

This test is for use in conjunction with the VerePLEX™ Biosystem.

One or more of the following targeted organisms can be identified with VereBeefTM Detection Kit:

•  Escherichia. coli O157:H7
•  non-O157 Shiga toxin-producing E. coli (STEC) serogroups
•  O26
•  O45
•  O103
•  O111
•  O121
•  O145
•  Salmonella species
The virulence genes targeted for E.coli analysis are:
•  eae (intimin)
•  stx (Shiga-like toxins)

VereFoodborne™ Detection Kit is a multiplex test combining both Polymerase Chain Reaction (PCR) and microarray technologies into a single testing workflow. This product is intended for qualitative detection, differentiation and identification of major food pathogens in a single test. This is a Research Use Only (RUO) test.

This test is for use in conjunction with the VerePLEX™ Biosystem.

One or more of the following targeted organisms can be identified with VereFoodborne™ Detection Kit:

•  Bacillus species
•  Campylobacter jejuni / lari / coli
•  Clostridium perfringens
•  Cronobacter sakazakii
•  Listeria species
•  Salmonella species
•  Shiga toxin-producing Escherichia Coli (STEC)
•  Shigella species
•  Staphylococcus aureus
•  Vibrio cholera
•  Vibrio parahaemolyticus
•  Shiga toxin genes (stx1A, stx2A)

VereFever™ Detection Kit is a multiplex test combining both Polymerase Chain Reaction (PCR) and microarray technologies into a single testing workflow. This product is intended for qualitative detection, differentiation and identification of multiple vector-borne pathogens in a single test. This is a Research Use Only (RUO) test.

This test is for use in conjunction with the VerePLEX™ Biosystem.

One or more of the following targeted organisms can be identified with VereFever™ Detection Kit:

•  Malaria parasites
     •  Plasmodium falciparum
     •  Plasmodium vivax
     •  Plasmodium malariae
     •  Plasmodium ovale
     •  Plasmodium knowlesi
•  Chikungunya virus
•  Dengue virus serotypes (1-4)
•  Japanese Encephalitis virus
•  West Nile virus
•  Yellow Fever virus
•  Zika virus

VereFluPlus™ Detection Kit is a multiplex test combining both Polymerase Chain Reaction (PCR) and microarray technologies into a single testing workflow. This product is intended for the qualitative detection, differentiation and identification of Influenza A and/or Influenza B virus in a single test. This is a Research Use Only (RUO) test.

This test is for use in conjunction with the VerePLEX™ Biosystem.

Based on a test matrix concept, one or more of the following targets can be identified with VereFluPlus™ Detection Kit:

•  Influenza A
•  Influenza B
•  H1
•  H3
•  H5
•  H7
•  H9
•  N1
•  N2
•  N6
•  N8
•  N9

VereMTB™ Detection Kit is a multiplex test combining both Polymerase Chain Reaction (PCR) and microarray technologies into a single testing workflow. This product is intended for qualitative detection, differentiation and identification of multiple pathogens in a single test. This is a Research Use Only (RUO) test.
This test is for use in conjunction with the VerePLEX™ Biosystem.

One or more of the following targets can be identified with VereMTB™ Detection Kit:

•  Mycobacterium tuberculosis complex (MTBC)
•  Mycobacterium tuberculosis (MTB) resistance or sensitivity to
•  Rifampicin
•  Isoniazid

The test also detects and differentiates 14 nontuberculous mycobacteria (NTM) consisting of
•  M. abscessus, M. chelonae
•  M. avium
•  M. intracellulare, M. vulneris, M.chimaera, M.colombiense
•  M. simiae, M. kansasii, M. scrofulaceum, M. gastri, M. mantenii
•  M. xenopi
•  M. fortuitum

VereThreat™ Detection Kit is a multiplex test combining both Polymerase Chain Reaction (PCR) and microarray technologies into a single testing workflow. This product is intended for qualitative detection, differentiation and identification of biological agents in a single test. This is a Research Use Only (RUO) test.

This test is for use in conjunction with the VerePLEX™ Biosystem.

One or more of the following targets can be identified with VereThreat™ Detection Kit:

•  Bacillus anthracis
•  Francisella tularensis
•  Yersinia pestis
•  Variola virus

VereMERS™ Detection Kit is a multiplex test combining both Polymerase Chain Reaction (PCR) and microarray technologies into a single testing workflow. This product is intended for the qualitative detection and identification of Middle East Respiratory Syndrome Coronavirus (MERS-CoV) in a single test. This is a Research Use Only (RUO) test.

This test is for use in conjunction with the VerePLEX™ Biosystem

VereCoV™ OneMix Detection Kit is a multiplex Reverse Transcription Polymerase Chain Reaction (RT-PCR)-based In Vitro Diagnostic (IVD) COVID-19 test intended for the qualitative detection of nucleic acid belonging to SARS-CoV-2. This test is for use in conjunction with VerePLEX™ Biosystem and the test results can be used as supplementary data for diagnosis. Negative result does not preclude SARS-CoV-2 infection and should not be used as a sole basis for treatment or other patient management decisions. Testing with VereCoV™ OneMix Detection Kit is intended for use by trained laboratory professionals who are proficient in using the VerePLEX™ Biosystem.

VereCoV™ OneMix Detection Kit is an improvement to VereCoV™ Detection Kit which is under Provisional Authorisation for IVD use issued by Health Sciences Authority (HSA) Singapore. This kit is also CE-IVD marked.

Compatibility
• CommaXP® Virus DNA / RNA Extraction Kit
• QIAamp® Viral RNA Mini Kit

Gene Targets
• ORF1ab
• Spike (S)
• Nucleocapsid (N)

Sensitivity
• 20 viral RNA copies per test

Turnaround Time
• Approximately 120 mins

VereRT™ ZeroPrep™ COVID-19 PCR Kit is a one-step Reverse Transcription Polymerase Chain Reaction (RT-PCR)-based In Vitro Diagnostic (IVD) COVID-19 test intended for the qualitative detection of nucleic acid belonging to SARS-CoV-2.

This test is suitable for use directly from either (1) Viral Transport Media (VTM) / Universal Transport Media (UTM) containing nasopharyngeal swab specimen; OR (2) Human saliva specimen. Both specimen types do not require viral RNA extraction prior to testing and the test results can be used as supplementary data for diagnosis. Negative result does not preclude SARS-CoV-2 infection and should not be used as a sole basis for treatment or other patient management decisions. Testing with VereRT™ ZeroPrep™ COVID-19 PCR Kit is intended for use by trained laboratory professionals who are proficient in performing real-time RT-PCR assays.

VereRT™ ZeroPrep™ COVID-19 PCR Kit is under Provisional Authorisation for IVD use issued by Health Sciences Authority (HSA) Singapore. Veredus is authorised to supply VereRT™ ZeroPrep™ COVID-19 PCR Kit to the healthcare institutions, private hospitals, medical clinics or clinics laboratories under the PHMC Act (Cap. 248) for use on their patients. This kit is also CE-IVD marked.

Veredus is authorised to export VereRT™ ZeroPrep™ COVID-19 PCR Kit out of Singapore subject to the duties and obligations as stipulated in the Health Products Act and the Health Products (Medical Devices) Regulation 2010.

Compatibility
• VTM* / UTM* containing nasopharyngeal swab specimen
• Human saliva specimen collected using ZeroPrep™ Saliva Collection Kit
* validated with 5 different brands of VTM /UTM

Gene Targets
• Dual N gene targets (FAM)
• Human RPP30 (HEX)

Sensitivity
• 10 viral RNA copies per test

Turnaround Time
• Approximately 90 mins

ZeroPrep™ Saliva Collection Kit is a specimen device intended for the collection of human saliva with the preservation buffer designed to protect and preserve viral RNA suitable for use directly in genetic and molecular diagnostic testing. This kit is compatible for use together with the VereRT™ ZeroPrep™ COVID-19 PCR Kit for the diagnosis of COVID-19.

ZeroPrep™ Saliva Collection Kit is registered as a Class A Medical Device with the Health Sciences Authority (HSA) Singapore.

Veredus is authorised to export ZeroPrep™ Saliva Collection Kit out of Singapore subject to the duties and obligations as stipulated in the Health Products Act and the Health Products (Medical Devices) Regulation 2010.

Compatibility
• VereRT™ ZeroPrep™ COVID-19 PCR Kit