Other products from "LUMINEX CORPORATION"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00840487101803 40-50035 Sheath Fluid PLUS is the delivery medium of the sample to the optics component. NSU Instrumentation for clinical multiplex test systems 2 xMAP® Sheath Fluid PLUS
2 00840487101797 40-50020 The MAGPIX Drive Fluid PLUS serves as the delivery medium that carries the sampl The MAGPIX Drive Fluid PLUS serves as the delivery medium that carries the sample to the optics component of the MAGPIX instrument. NSU Instrumentation for clinical multiplex test systems 2 MAGPIX® Drive Fluid PLUS (4PK)
3 00840487101315 3909 3909 Nucleic acid sequences, which, through specific binding or chemical reaction wit Nucleic acid sequences, which, through specific binding or chemical reaction with substances in a specimen, are intended for use in a diagnostic application for identification and quantification of an individual chemical substance or ligand in biological specimens MVU REAGENTS,SPECIFIC,ANALYTE 1 MultiCode® EBV Primers
4 00840487101742 3928 3928 Nucleic acid sequences, which, through specific binding or chemical reaction wit Nucleic acid sequences, which, through specific binding or chemical reaction with substances in a specimen, are intended for use in a diagnostic application for identification and quantification of an individual chemical substance or ligand in biological specimens MVU REAGENTS,SPECIFIC,ANALYTE 1 Multicode® Mycoplasma genitalium Primers
5 00840487101612 20-006-024 20-006-024 The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multip The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multiplexed qualitative test intended for the simultaneous detection and identification of multiple viral and bacterial nucleic acids in nasopharyngeal swabs (NPS) obtained from individuals suspected of respiratory tract infection. OCC,OZE,OZZ,OEM,OOU,OEP Respiratory virus panel nucleic acid assay system,Influenza A and influenza B mu Respiratory virus panel nucleic acid assay system,Influenza A and influenza B multiplex nucleic acid assay,Bordetella pertussis dna assay system,Human metapneumovirus (hmpv) rna assay system,Parainfluenza multiplex nucleic acid assay,Influenza a virus subtype differentiation nucleic acid assay 2 Respiratory Pathogens Flex (RP Flex) Nucleic Acid Test Cartridge
6 00840487101544 20-011-023 20-011-023 The Verigene® Enteric Pathogens Nucleic Acid Test (EP) is a multiplexed, qualita The Verigene® Enteric Pathogens Nucleic Acid Test (EP) is a multiplexed, qualitative test for simultaneous detection and identification of common pathogenic enteric bacteria, viruses, and genetic virulence markers from liquid or soft stool preserved in Cary-Blair medium, collected from individuals with signs and symptoms of gastrointestinal infection. PCH,PCI Gastrointestinal pathogen panel multiplex nucleic acid-based assay system,Gastro Gastrointestinal pathogen panel multiplex nucleic acid-based assay system,Gastrointestinal bacterial panel multiplex nucleic acid-based assay system 2 Enteric Pathogens (EP) Amplification Tray
7 00840487101506 10-0000-04 10-0000-04 The Verigene® Processor is an instrument which internalizes all of the functions The Verigene® Processor is an instrument which internalizes all of the functions required to process a Test Cartridge as part of the Verigene® System, a benchtop molecular diagnostics workstation that utilizes patented gold nanoparticle technology to detect nucleic acid targets of interest for a variety of applications. NSU Instrumentation for clinical multiplex test systems 2 Verigene® Processor
8 00840487101490 10-0000-07R 10-0000-07R The Verigene® Processor SP is an instrument which integrates sample preparation, The Verigene® Processor SP is an instrument which integrates sample preparation, target amplification, and target hybridization within a single device as part of the Verigene® System, a benchtop molecular diagnostics workstation that utilizes patented gold nanoparticle technology to detect nucleic acid targets of interest for a variety of applications. (Refurbished) NSU,OOI Instrumentation for clinical multiplex test systems,real time Nucleic acid ampli Instrumentation for clinical multiplex test systems,real time Nucleic acid amplification system 2 Verigene® Processor SP (Refurbished)
9 00840487101216 3804-22 3804-22 Internal control used in real-time polymerase chain reaction (pcr) assays to det Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes. OLD Internal polymerase chain reaction control, not assay specific 1 MHV Control Primers 3
10 00840487101209 3804-21 3804-21 Internal control used in real-time polymerase chain reaction (pcr) assays to det Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes. OLD Internal polymerase chain reaction control, not assay specific 1 MHV Control Primers 3
11 00840487101193 3804 3804 Internal control used in real-time polymerase chain reaction (pcr) assays to det Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes. OLD Internal polymerase chain reaction control, not assay specific 1 MHV Control Primers 3
12 00840487101186 3803-21 3803-21 Internal control used in real-time polymerase chain reaction (pcr) assays to det Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes. OLD Internal polymerase chain reaction control, not assay specific 1 MHV Control Primers 2
13 00840487101179 3803 3803 Internal control used in real-time polymerase chain reaction (pcr) assays to det Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes. OLD Internal polymerase chain reaction control, not assay specific 1 MHV Control Primers 2
14 00840487100332 LX200-CON-K25 xMAP Control Microspheres, Classification (CON1) and Reporter (CON2), are polyst xMAP Control Microspheres, Classification (CON1) and Reporter (CON2), are polystyrene microspheres that are internally labeled with fluorescent dyes. The control microspheres are intended to verify the calibration and optical integrity for the Luminex 100/200 System. Classification Control Microspheres verify both classification channels and the doublet discriminator channel (DD). Reporter Control Microspheres verify the reporter channel. NSU Instrumentation for clinical multiplex test systems 2 Luminex® 100/200™ Performance Verification Kit
15 00840487100288 MPXIVD-PVER-K25 The Luminex MAGPIX Performance Verification Kit is intended to verify the optica The Luminex MAGPIX Performance Verification Kit is intended to verify the optical calibration of the MAGPIX instrument. NSU Instrumentation for clinical multiplex test systems 2 MAGPIX® Performance Verification Kit
16 00840487100271 MPXIVD-CAL-K25 The Luminex MAGPIX Calibration Kit is intended to calibrate the optics of the MA The Luminex MAGPIX Calibration Kit is intended to calibrate the optics of the MAGPIX instrument. During calibration, the system adjusts LED current and calibration factors for CL1, CL2, and RP1 until those values match the imported target values, thus calibrating the classification map. NSU Instrumentation for clinical multiplex test systems 2 MAGPIX® Calibration Kit
17 00840487100158 50-10020 The ARIES® Flu A/B & RSV Assay is a polymerase chain reaction (PCR) based qualit The ARIES® Flu A/B & RSV Assay is a polymerase chain reaction (PCR) based qualitative in vitro diagnostic test for the direct detection and differentiation of influenza A virus, influenza B virus, and respiratory syncytial virus (RSV) nucleic acid in nasopharyngeal swabs (NPS) specimens from patients with signs and symptoms of respiratory tract infection in conjunction with clinical and laboratory findings. OZE,OCC Influenza A and influenza B multiplex nucleic acid assay,Respiratory virus panel Influenza A and influenza B multiplex nucleic acid assay,Respiratory virus panel nucleic acid assay system 2 ARIES® Flu A/B & RSV Assay
18 00840487100080 ARIES M6V1 The ARIES® M1 System is a clinical multiplex test system that automates and inte The ARIES® M1 System is a clinical multiplex test system that automates and integrates extraction of nucleic acid from a clinical sample, performs real -time PCR, and measuring and sorting multiple signals generated in an in vitro diagnostic assay. OOI real time Nucleic acid amplification system 2 ARIES® M1 System
19 00840487101766 VERIGENE-II-6M-IVD The VERIGENE® II System is an in vitro diagnostic (IVD) platform that performs n The VERIGENE® II System is an in vitro diagnostic (IVD) platform that performs nucleic acid based tests in clinical laboratories. The VERIGENE II System is capable of automated extraction and purification of nucleic acids from multiple sample types as well as automated amplification, array hybridization, and detection of target nucleic acid sequences. NSU Instrumentation for clinical multiplex test systems 2 VERIGENE® II System
20 00840487101711 20-011-024 20-011-024 The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multip The Verigene® Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) is a multiplexed qualitative test intended for the simultaneous detection and identification of multiple viral and bacterial nucleic acids in nasopharyngeal swabs (NPS) obtained from individuals suspected of respiratory tract infection. OEP,OCC,OZZ,OZE,OEM,OOU Influenza a virus subtype differentiation nucleic acid assay,Respiratory virus p Influenza a virus subtype differentiation nucleic acid assay,Respiratory virus panel nucleic acid assay system,Bordetella pertussis dna assay system,Influenza A and influenza B multiplex nucleic acid assay,Human metapneumovirus (hmpv) rna assay system,Parainfluenza multiplex nucleic acid assay 2 Respiratory Pathogens Flex (RP Flex) Amplification Tray
21 00840487101377 3916 3916 Nucleic acid sequences, which, through specific binding or chemical reaction wit Nucleic acid sequences, which, through specific binding or chemical reaction with substances in a specimen, are intended for use in a diagnostic application for identification and quantification of an individual chemical substance or ligand in biological specimens MVU REAGENTS,SPECIFIC,ANALYTE 1 MultiCode® VZV Primers
22 00840487101353 3914 3914 Nucleic acid sequences, which, through specific binding or chemical reaction wit Nucleic acid sequences, which, through specific binding or chemical reaction with substances in a specimen, are intended for use in a diagnostic application for identification and quantification of an individual chemical substance or ligand in biological specimens MVU REAGENTS,SPECIFIC,ANALYTE 1 MultiCode® Adenovirus Primers
23 00840487101162 3802-21 3802-21 Internal control used in real-time polymerase chain reaction (pcr) assays to det Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes. OLD Internal polymerase chain reaction control, not assay specific 1 MHV Control Primers 1
24 00840487101155 3802 3802 Internal control used in real-time polymerase chain reaction (pcr) assays to det Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes. OLD Internal polymerase chain reaction control, not assay specific 1 MHV Control Primers 1
25 00840487101124 3694-22 3694-22 Internal control used in real-time polymerase chain reaction (pcr) assays to det Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes. OLD Internal polymerase chain reaction control, not assay specific 1 MHV DNA Amplification Control
26 00840487101117 3694-21 3694-21 Internal control used in real-time polymerase chain reaction (pcr) assays to det Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes. OLD Internal polymerase chain reaction control, not assay specific 1 MHV DNA Amplification Control
27 00840487101100 3694 3694 Internal control used in real-time polymerase chain reaction (pcr) assays to det Internal control used in real-time polymerase chain reaction (pcr) assays to detect systemic variation that may arise during the extraction and amplification process associated with real-time pcr assays. It is not intended to monitor other real-time pcr processes. OLD Internal polymerase chain reaction control, not assay specific 1 MHV DNA Amplification Control
28 00840487100257 3927 3927 Nucleic acid sequences, which, through specific binding or chemical reaction wit Nucleic acid sequences, which, through specific binding or chemical reaction with substances in a specimen, are intended for use in a diagnostic application for identification and quantification of an individual chemical substance or ligand in biological specimens MVU REAGENTS,SPECIFIC,ANALYTE 1 MultiCode® Mycoplasma pneumoniae Primers
29 00840487100219 3923 3923 Nucleic acid sequences, which, through specific binding or chemical reaction wit Nucleic acid sequences, which, through specific binding or chemical reaction with substances in a specimen, are intended for use in a diagnostic application for identification and quantification of an individual chemical substance or ligand in biological specimens MVU REAGENTS,SPECIFIC,ANALYTE 1 MultiCode® Group A Strep Primers
30 00840487100073 50-10026 The ARIES® Extraction Kit is intended to extract nucleic acid from human biologi The ARIES® Extraction Kit is intended to extract nucleic acid from human biological specimens and universal transport media (UTM). OOI real time Nucleic acid amplification system 2 ARIES® Extraction Kit
31 00840487101780 40-50036 A concentrated version of xMAP® Sheath Fluid PLUS, when diluted is is the delive A concentrated version of xMAP® Sheath Fluid PLUS, when diluted is is the delivery medium of the sample to the optics component. NSU Instrumentation for clinical multiplex test systems 2 xMAP® Sheath Concentrate PLUS
32 00840487101735 30-002-022 30-002-022 The Verigene® Clostridium difficile Nucleic Acid Test (CDF) is a qualitative mul The Verigene® Clostridium difficile Nucleic Acid Test (CDF) is a qualitative multiplexed in vitro diagnostic test for the rapid detection of toxin A (tcdA), toxin B (tcdB), and tcdC gene sequences of toxigenic Clostridium difficile and for presumptive identification of PCR ribotype 027 strains from unformed (liquid or soft) stool specimens collected from patients suspected of having C. difficile infection (CDI). OZN C. Difficile toxin gene amplification assay 2 Clostridium difficile (CDF) Stool Sample Preparation Kit
33 00840487101643 20-009-021 20-009-021 The Verigene® Gram-Negative Blood Culture Nucleic Acid Test (BC-GN) performed us The Verigene® Gram-Negative Blood Culture Nucleic Acid Test (BC-GN) performed using the sample-to-result Verigene® System, is a qualitative multiplexed in vitro diagnostic test for the simultaneous detection and identification of selected gram-negative bacteria and resistance markers. PEN Gram-Negative bacteria and associated resistance markers 2 Gram-Negative Blood Culture (BC-GN) Extraction Tray
34 00840487101278 3906-21 3906-21 Nucleic acid sequences, which, through specific binding or chemical reaction wit Nucleic acid sequences, which, through specific binding or chemical reaction with substances in a specimen, are intended for use in a diagnostic application for identification and quantification of an individual chemical substance or ligand in biological specimens MVU REAGENTS,SPECIFIC,ANALYTE 1 MultiCode® CMV Primers
35 00840487101261 3906 3906 Nucleic acid sequences, which, through specific binding or chemical reaction wit Nucleic acid sequences, which, through specific binding or chemical reaction with substances in a specimen, are intended for use in a diagnostic application for identification and quantification of an individual chemical substance or ligand in biological specimens MVU REAGENTS,SPECIFIC,ANALYTE 1 MultiCode® CMV Primers
36 00840487101230 3901 3901 Nucleic acid sequences, which, through specific binding or chemical reaction wit Nucleic acid sequences, which, through specific binding or chemical reaction with substances in a specimen, are intended for use in a diagnostic application for identification and quantification of an individual chemical substance or ligand in biological specimens MVU REAGENTS,SPECIFIC,ANALYTE 1 MultiCode® Bordetella pertussis Primers
37 00840487101223 3900 3900 Nucleic acid sequences, which, through specific binding or chemical reaction wit Nucleic acid sequences, which, through specific binding or chemical reaction with substances in a specimen, are intended for use in a diagnostic application for identification and quantification of an individual chemical substance or ligand in biological specimens MVU REAGENTS,SPECIFIC,ANALYTE 1 MultiCode® HSV Primers
38 00840487100295 50-10017 The ARIES® HSV 1 & 2 Assay is a polymerase chain reaction (PCR)-based qualitativ The ARIES® HSV 1 & 2 Assay is a polymerase chain reaction (PCR)-based qualitative in vitro diagnostic test for the direct detection and differentiation of herpes simplex virus (HSV) DNA from cutaneous and mucocutaneous lesion swab specimens. PGI Herpes virus (VZV, HSV1, HSV2), DNA Detection Assay for cutaneous and mucocutane Herpes virus (VZV, HSV1, HSV2), DNA Detection Assay for cutaneous and mucocutaneous lesion samples 2 ARIES® HSV 1&2 Assay
39 00840487100097 40-50000 Sheath fluid is the delivery medium of the sample to the optics component. NSU Instrumentation for clinical multiplex test systems 2 xMAP® Sheath Fluid
40 00840487101674 20-011-018 20-011-018 The Verigene® Gram-Positive Blood Culture Nucleic Acid Test (BC-GP) performed us The Verigene® Gram-Positive Blood Culture Nucleic Acid Test (BC-GP) performed using the sample-to-result Verigene® System is a qualitative, multiplexed in vitro diagnostic test for the simultaneous detection and identification of potentially pathogenic gram-positive bacteria which may cause bloodstream infection (BSI). NQX,PAM SYSTEM, NUCLEIC ACID AMPLIFICATION TEST, DNA, METHICILLIN RESISTANT STAPHYLOCOCC SYSTEM, NUCLEIC ACID AMPLIFICATION TEST, DNA, METHICILLIN RESISTANT STAPHYLOCOCCUS AUREUS, DIRECT SPECIMEN,Gram-positive bacteria and their resistance markers 2 Gram-Positive Blood Culture (BC-GP) Utility Tray
41 00840487101599 20-006-021 20-006-021 The Verigene® Gram-Negative Blood Culture Nucleic Acid Test (BC-GN) performed us The Verigene® Gram-Negative Blood Culture Nucleic Acid Test (BC-GN) performed using the sample-to-result Verigene® System, is a qualitative multiplexed in vitro diagnostic test for the simultaneous detection and identification of selected gram-negative bacteria and resistance markers. PEN Gram-Negative bacteria and associated resistance markers 2 Gram-Negative Blood Culture (BC-GN) Nucleic Acid Test Cartridge
42 00840487101469 50-10041 The ARIES® Group A Strep Assay is a real-time polymerase chain reaction (PCR) ba The ARIES® Group A Strep Assay is a real-time polymerase chain reaction (PCR) based qualitative in vitro diagnostic test for the direct detection of Streptococcus pyogenes (Group A ß-hemolytic Streptococcus) in throat swab specimens from patients with signs and symptoms of pharyngitis. PGX,OOI Groups A, C and G beta-hemolytic streptococcus nucleic acid amplification system Groups A, C and G beta-hemolytic streptococcus nucleic acid amplification system,real time Nucleic acid amplification system 2 ARIES® Group A Strep Assay
43 00840487101421 MPXDF-4PK-1 The MAGPIX Drive Fluid serves as the delivery medium that carries the sample to The MAGPIX Drive Fluid serves as the delivery medium that carries the sample to the optics component of the MAGPIX instrument. NSU Instrumentation for clinical multiplex test systems 2 MAGPIX® Drive Fluid
44 00840487101032 3711 3711 The MultiCode®-RTx Herpes Simplex Virus 1 & 2 Kit is a polymerase chain reaction The MultiCode®-RTx Herpes Simplex Virus 1 & 2 Kit is a polymerase chain reaction (PCR)-based qualitative in vitro diagnostic test for the detection and typing of herpes simplex virus (HSV 1 & 2) DNA in vaginal lesions. It is indicated for use in the detection and typing of HSV-1 or HSV-2 in vaginal lesion swab specimens from symptomatic female patients as an aid in the diagnosis of genital herpes infection. OQO Herpes simplex virus nucleic acid amplification assay 2 Mutlicode®-RTx HSV 1&2 Kit
45 00840487100448 CN-SW47 The SYNCT Software is a desktop application that can be utilized by an end-user The SYNCT Software is a desktop application that can be utilized by an end-user on a standalone computer, providing users the ability to operate general functions such as Order Management, with or without a Laboratory Information System (LIS), viewing test results, reviewing and preparing test reports, performing software administrative functions, and providing security control for permitted functions. OOI real time Nucleic acid amplification system 2 SYNCT™ Software
46 00840487100325 10-0000-02 10-0000-02 The Verigene® Reader is the central control of the Verigene® System, a benchtop The Verigene® Reader is the central control of the Verigene® System, a benchtop molecular diagnostics workstation that utilizes patented gold nanoparticle technology to detect nucleic acid targets of interest for a variety of applications. OOI,NSU real time Nucleic acid amplification system,Instrumentation for clinical multipl real time Nucleic acid amplification system,Instrumentation for clinical multiplex test systems 2 Verigene® Reader
47 00840487100059 50-10018 The ARIES® C. difficile Assay is a real-time polymerase chain reaction (PCR) bas The ARIES® C. difficile Assay is a real-time polymerase chain reaction (PCR) based qualitative in vitro diagnostic test for the direct detection of Clostridium difficile (C. difficile) nucleic acid in unformed (liquid or soft) stool specimens obtained from patients suspected of having Clostridium difficile infection (CDI). OZN C.Difficile toxin gene amplification assay 2 ARIES® C. difficile Assay
48 00840487101728 30-001-001 30-001-001 The Verigene® Hypercoagulation Panel Nucleic Acid Test contains the Verigene® F The Verigene® Hypercoagulation Panel Nucleic Acid Test contains the Verigene® F5 Nucleic Acid Test, the Verigene® F2 Nucleic Acid Test and the Verigene® MTHFR Nucleic Acid Test. The Verigene® F5 Nucleic Acid Test is an in vitro diagnostic for the detection and genotyping of a single point mutation (G to A at position 1691; also known as Factor V Leiden) of the human Factor V gene (F5; Coagulation Factor V gene) in patients with suspected thrombophilia, from isolated genomic DNA obtained from whole blood samples. The Verigene® F2 Nucleic Acid Test is an in vitro diagnostic for the detection and genotyping of a single point mutation (G to A at position 20210) of the human Factor II gene (F2; prothrombin gene) in patients with suspected thrombophilia, from isolated genomic DNA obtained from whole blood samples. The Verigene® MTHFR Nucleic Acid Test is an in vitro diagnostic for the detection and genotyping of a single point mutation (C to T at position 677) of the human 5,10 methylenetetrahydrofolate reductase gene (MTHFR) in patients with suspected thrombophilia, from isolated genomic DNA obtained from whole blood samples. OMM,NPQ,NPR Test 5, 10-methylenetetrahydrofolate reductase mutations, genomic dna pcr,TEST, Test 5, 10-methylenetetrahydrofolate reductase mutations, genomic dna pcr,TEST, FACTOR V LEIDEN MUTATIONS, GENOMIC DNA PCR,TEST, FACTOR II G20210A MUTATIONS, GENOMIC DNA PCR 2 Hypercoagulation Panel (HC) Sample Buffer
49 00840487101537 ARIES M12V1 The ARIES® System is a clinical multiplex test system that automates and integra The ARIES® System is a clinical multiplex test system that automates and integrates extraction of nucleic acid from a clinical sample, performs real -time PCR, and measuring and sorting multiple signals generated in an in vitro diagnostic assay. OOI real time Nucleic acid amplification system 2 ARIES® System
50 00840487101476 10-0000-02R 10-0000-02R The Verigene® Reader is the central control of the Verigene® System, a benchtop The Verigene® Reader is the central control of the Verigene® System, a benchtop molecular diagnostics workstation that utilizes patented gold nanoparticle technology to detect nucleic acid targets of interest for a variety of applications. (Refurbished) OOI,NSU real time Nucleic acid amplification system,Instrumentation for clinical multipl real time Nucleic acid amplification system,Instrumentation for clinical multiplex test systems 2 Verigene® Reader (Refurbished)
Other products with the same Product Code "MVU"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00816879026559 F255 743140 Plum, Prunus domestica HYCOR BIOMEDICAL LLC
2 00816879026542 G202 743340 Corn, Cultivated, Zea mays HYCOR BIOMEDICAL LLC
3 00816879026535 I71 743560 Mosquito, Aedes communis HYCOR BIOMEDICAL LLC
4 00816879026528 O1 743990 Cotton Linters (Untreated) HYCOR BIOMEDICAL LLC
5 00816879026511 T49 744050 Pine, Ponderosa, Pinus ponderosa HYCOR BIOMEDICAL LLC
6 00816879026504 T96 744100 White Poplar, Populus alba HYCOR BIOMEDICAL LLC
7 00816879026498 T228 744770 Aspen, Quaking, Populus tremoloides HYCOR BIOMEDICAL LLC
8 00816879026481 M215 744910 Corn Smut, Ustilago maydis HYCOR BIOMEDICAL LLC
9 00816879026474 I70 745370 Fire Ant, Solenopsis invicta HYCOR BIOMEDICAL LLC
10 00816879026467 F67 745760 Parmesan Cheese HYCOR BIOMEDICAL LLC
11 00816879026450 F281 745920 Curry HYCOR BIOMEDICAL LLC
12 00816879026443 F265 745930 Cumin, Cuminum cyminum HYCOR BIOMEDICAL LLC
13 00816879026436 F237 746030 Apricot, Prunus armeniaca HYCOR BIOMEDICAL LLC
14 00816879026429 F177 746070 Cranberry, Vaccinium macrocarpon HYCOR BIOMEDICAL LLC
15 00816879026412 F247 746280 Honey HYCOR BIOMEDICAL LLC
16 00816879026405 F336 746290 Wine Vinegar HYCOR BIOMEDICAL LLC
17 00816879026399 F157 746360 Duck HYCOR BIOMEDICAL LLC
18 00816879026382 F19 746550 Cayenne Pepper, Capsicum frutescens HYCOR BIOMEDICAL LLC
19 00816879026375 F198 746600 Linseed/Flaxseed HYCOR BIOMEDICAL LLC
20 00816879026368 F50 746660 Mackerel, Scomber japonicus HYCOR BIOMEDICAL LLC
21 00816879026351 F234 746780 Vanilla, Vanilla planifolia HYCOR BIOMEDICAL LLC
22 00816879026344 F268 746830 Cloves, Syzygium aromaticum HYCOR BIOMEDICAL LLC
23 00816879026337 F282 746870 Nutmeg, Myristica fragrans HYCOR BIOMEDICAL LLC
24 00816879026320 F221 74280 Coffee, Coffea spp. HYCOR BIOMEDICAL LLC
25 00816879026313 F280 74290 Black Pepper, Piper nigrum HYCOR BIOMEDICAL LLC
26 00816879026306 F94 74291 Pear, Pyrus communis HYCOR BIOMEDICAL LLC
27 00816879026290 F244 74297 Cucumber, Cucumis sativus HYCOR BIOMEDICAL LLC
28 00816879026283 F11 74302 Buckwheat, Fagopyrum esculentum HYCOR BIOMEDICAL LLC
29 00816879026276 F90 74303 Malt HYCOR BIOMEDICAL LLC
30 00816879026269 F315 74305 Green Bean, Phaseolus vulgaris HYCOR BIOMEDICAL LLC
31 00816879026252 F152 74315 Green Bell Pepper, Capsicum annuum HYCOR BIOMEDICAL LLC
32 00816879026245 F260 74570 Broccoli, Brassica oleracea var. botrytis HYCOR BIOMEDICAL LLC
33 00816879026238 F360 74574 Yogurt HYCOR BIOMEDICAL LLC
34 00816879026221 F29 74578 Watermelon, Citrullus vulgaris HYCOR BIOMEDICAL LLC
35 00816879026214 F214 74581 Spinach, Spinacia oleracea HYCOR BIOMEDICAL LLC
36 00816879026207 F155 74583 Brewer's Yeast, Saccharomyces cerevisiae HYCOR BIOMEDICAL LLC
37 00816879026191 F209 74611 Grapefruit, Citrus paradisi HYCOR BIOMEDICAL LLC
38 00816879026184 F84 74650 Kiwi, Actinidia chinensis HYCOR BIOMEDICAL LLC
39 00816879026177 F86 74651 Parsley, Petrosilenum crispum HYCOR BIOMEDICAL LLC
40 00816879026160 F87 74654 Melon, Honeydew, Cucumis melo HYCOR BIOMEDICAL LLC
41 00816879026153 F91 74656 Mango, Mangifera indica HYCOR BIOMEDICAL LLC
42 00816879026146 F95 74657 Peach, Prunus persica HYCOR BIOMEDICAL LLC
43 00816879026139 F207 74667 Clam, Mercenaria mercenaria HYCOR BIOMEDICAL LLC
44 00816879026115 F377 741090 Maple Syrup HYCOR BIOMEDICAL LLC
45 00816879026108 F299 742430 Sweet Chestnut, Castanea sativa HYCOR BIOMEDICAL LLC
46 00816879026092 F53 742680 Scallop HYCOR BIOMEDICAL LLC
47 00816879026085 F88 742790 Lamb, Ovis aries HYCOR BIOMEDICAL LLC
48 00816879026078 F242 743210 Bing Cherry, Prunus avium HYCOR BIOMEDICAL LLC
49 00816879026061 W45 745050 Alfalfa, Medicago sativa HYCOR BIOMEDICAL LLC
50 00816879026054 F136 745640 Red Beet, Beta vulgaris HYCOR BIOMEDICAL LLC