Other products from "FUJIFILM WAKO PURE CHEMICAL CORPORATION"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00856626006151 997-43801 997-43801 In-Vitro Diagnostic Use DAE Complement C9, Antigen, Antiserum, Control 2 CH50 Calibrator
2 14987481164595 993-72691 993-72691 In-Vitro Diagnostic Use LBR Ldl & Vldl Precipitation, Hdl 1 L-Type HDL-C Reagent 2
3 14987481164571 997-00201 997-00201 In-Vitro Diagnostic Use JIS Calibrator, Primary 2 L-Type HDL-C Reagent 2
4 14987481164427 993-61601 993-61601 The uTASWako chip cassette is designed to be used for the assays on the uTASWako i30. NSF Test, Alpha Fetoprotein L3 Subfraction (Afp-L3%), For Hepatocellular Carcinoma R Test, Alpha Fetoprotein L3 Subfraction (Afp-L3%), For Hepatocellular Carcinoma Risk Assessment 2 uTASWako Chip Cassette
5 10856626006097 993-72691 993-72691 In-Vitro Diagnostic Use LBR Ldl & Vldl Precipitation, Hdl L-Type HDL-C Reagent 2
6 10856626006080 993-61601 993-61601 The uTASWako chip cassette is designed to be used for the assays on the uTASWako i30. NSF Test, Alpha Fetoprotein L3 Subfraction (Afp-L3%), For Hepatocellular Carcinoma R Test, Alpha Fetoprotein L3 Subfraction (Afp-L3%), For Hepatocellular Carcinoma Risk Assessment uTASWako Chip Cassette
7 04987481164673 991-06201 991-06201 In-Vitro Diagnostic Use JJX Single (Specified) Analyte Controls (Assayed And Unassayed) 1 Autokit Micro Albumin Control Set
8 04987481164512 997-43801 997-43801 In-Vitro Diagnostic Use DAE Complement C9, Antigen, Antiserum, Control 2 CH50 Calibrator
9 00856626006106 995-06101 995-06101 In-Vitro Diagnostic Use JJX Single (Specified) Analyte Controls (Assayed And Unassayed) 1 Autokit Micro Albumin Calibrator Set
10 14987481164588 997-72591 997-72591 In-Vitro Diagnostic Use LBR Ldl & Vldl Precipitation, Hdl 1 L-Type HDL-C Reagent 1
11 14987481164564 991-00101 991-00101 In-Vitro Diagnostic Use JIS Calibrator, Primary 2 L-Type HDL-C Reagent 1
12 14987481164540 999-00504 999-00504 In-Vitro Diagnostic Use LBR Ldl & Vldl Precipitation, Hdl 1 L-Type LDL-C Reagent 2
13 04987481164529 995-06101 995-06101 In-Vitro Diagnostic Use JJX Single (Specified) Analyte Controls (Assayed And Unassayed) 1 Autokit Micro Albumin Calibrator Set
14 14987481164502 991-60801 991-60801 In-Vitro Diagnostic Use NSF Test, Alpha Fetoprotein L3 Subfraction (Afp-L3%), For Hepatocellular Carcinoma R Test, Alpha Fetoprotein L3 Subfraction (Afp-L3%), For Hepatocellular Carcinoma Risk Assessment 2 uTASWako Wash Solution
15 10856626006059 991-60801 991-60801 In-Vitro Diagnostic Use NSF Test, Alpha Fetoprotein L3 Subfraction (Afp-L3%), For Hepatocellular Carcinoma R Test, Alpha Fetoprotein L3 Subfraction (Afp-L3%), For Hepatocellular Carcinoma Risk Assessment uTASWako Wash Solution
16 10856626006042 991-00101 991-00101 The L-Type HDL-C is an in vitro assay for the quantitative determination of high The L-Type HDL-C is an in vitro assay for the quantitative determination of high density lipoprotein cholesterol (HDL-C) in serum. (4 each 600 mL) JIS Calibrator, Primary L-Type HDL-C (Reagent 1)
17 04987481164666 999-06001 999-06001 In-Vitro Diagnostic Use JIQ Turbidimetric Method, Protein Or Albumin (Urinary, Non-Quant.) 1 Autokit Micro Albumin
18 00856626006168 997-60901 997-60901 In-Vitro Diagnostic Use JIT Calibrator, Secondary 2 uTASWako AFP-L3 Calibrator Set
19 00856626006120 995-60701 995-60701 In-Vitro Diagnostic Use OAU Des-Gamma-Carboxy-Prothrombin (Dcp), Risk Assessment, Hepatocellular Carcinoma 2 uTASWako DCP
20 14987481164618 995-34791 995-34791 In-Vitro Diagnostic Use JLH Titrimetric, Fatty Acids 1 HR Series NEFA-HR(2) Solvent A
21 14987481164496 991-61401 991-61401 In-Vitro Diagnostic Use JJX Single (Specified) Analyte Controls (Assayed And Unassayed) 1 uTASWako DCP Control H
22 10856626006066 991-61401 991-61401 In-Vitro Diagnostic Use JJX Single (Specified) Analyte Controls (Assayed And Unassayed) uTASWako DCP Control H
23 04987481164437 997-60901 997-60901 In-Vitro Diagnostic Use JIT Calibrator, Secondary 2 uTASWako AFP-L3 Calibrator Set
24 04987481164413 995-60701 995-60701 In-Vitro Diagnostic Use OAU Des-Gamma-Carboxy-Prothrombin (Dcp), Risk Assessment, Hepatocellular Carcinoma 2 uTASWako DCP
25 14987481164632 993-35191 993-35191 In-Vitro Diagnostic Use JLH Titrimetric, Fatty Acids 1 HR Series NEFA-HR(2) Solvent B
26 14987481164489 995-61301 995-61301 In-Vitro Diagnostic Use JJX Single (Specified) Analyte Controls (Assayed And Unassayed) 1 uTASWako DCP Control L
27 14987481164458 993-61101 993-61101 In-Vitro Diagnostic Use JJX Single (Specified) Analyte Controls (Assayed And Unassayed) 1 uTASWako AFP-L3 Control H
28 10856626006134 995-61301 995-61301 In-Vitro Diagnostic Use JJX Single (Specified) Analyte Controls (Assayed And Unassayed) uTASWako DCP Control L
29 10856626006073 993-61101 993-61101 In-Vitro Diagnostic Use JJX Single (Specified) Analyte Controls (Assayed And Unassayed) uTASWako AFP-L3 Control H
30 00856626006205 999-60601 999-60601 In-Vitro Diagnostic Use NSF Test, Alpha Fetoprotein L3 Subfraction (Afp-L3%), For Hepatocellular Carcinoma R Test, Alpha Fetoprotein L3 Subfraction (Afp-L3%), For Hepatocellular Carcinoma Risk Assessment 2 uTASWako AFP-L3
31 14987481164601 999-34691 999-34691 In-Vitro Diagnostic Use JLH Titrimetric, Fatty Acids 1 HR Series NEFA-HR(2) Color Reagent A
32 14987481164557 990-28011 990-28011 In-Vitro Diagnostic Use JIS Calibrator, Primary 2 HDL-C/LDL-C Calibrator
33 14987481164441 997-61001 997-61001 In-Vitro Diagnostic Use JJX Single (Specified) Analyte Controls (Assayed And Unassayed) 1 uTASWako AFP-L3 Control L
34 14987481102924 464-01601 464-01601 In-Vitro Diagnostic Use JIX Calibrator, Multi-Analyte Mixture 2 Multi Calibrator Lipids
35 10856626006172 997-61001 997-61001 In-Vitro Diagnostic Use JJX Single (Specified) Analyte Controls (Assayed And Unassayed) uTASWako AFP-L3 Control L
36 10856626006141 997-00201 997-00201 The L-Type HDL-C is an in vitro assay for the quantitative determination of high The L-Type HDL-C is an in vitro assay for the quantitative determination of high density lipoprotein cholesterol (HDL-C) in serum. (4 each 600 mL) JIS Calibrator, Primary L-Type HDL-C (Reagent 2)
37 10856626006035 990-28011 990-28011 In-Vitro Diagnostic Use JIS Calibrator, Primary HDL-C/LDL-C Calibrator
38 10856626006028 464-01601 464-01601 In-Vitro Diagnostic Use JIX Calibrator, Multi-Analyte Mixture Multi Calibrator Lipids
39 04987481164642 997-76491 997-76491 In-Vitro Diagnostic Use JJX Single (Specified) Analyte Controls (Assayed And Unassayed) 1 NEFA Linearity Material
40 04987481164390 999-60601 999-60601 In-Vitro Diagnostic Use NSF Test, Alpha Fetoprotein L3 Subfraction (Afp-L3%), For Hepatocellular Carcinoma R Test, Alpha Fetoprotein L3 Subfraction (Afp-L3%), For Hepatocellular Carcinoma Risk Assessment 2 uTASWako AFP-L3
41 14987481164465 997-61501 997-61501 In-Vitro Diagnostic Use NSF Test, Alpha Fetoprotein L3 Subfraction (Afp-L3%), For Hepatocellular Carcinoma R Test, Alpha Fetoprotein L3 Subfraction (Afp-L3%), For Hepatocellular Carcinoma Risk Assessment 2 uTASWako AFP-L3 Sample Dilution Buffer
42 10856626006189 997-61501 997-61501 In-Vitro Diagnostic Use NSF Test, Alpha Fetoprotein L3 Subfraction (Afp-L3%), For Hepatocellular Carcinoma R Test, Alpha Fetoprotein L3 Subfraction (Afp-L3%), For Hepatocellular Carcinoma Risk Assessment uTASWako AFP-L3 Sample Dilution Buffer
43 00856626006229 991-60301 991-60301 In-Vitro Diagnostic Use OUE Micro Total Analysis Instrument System 2 uTASWako i30
44 00856626006212 999-61201 999-61201 In-Vitro Diagnostic Use JIT Calibrator, Secondary 2 uTASWako DCP Calibrator Set
45 00856626006113 995-40801 995-40801 In-Vitro Diagnostic Use DAE Complement C9, Antigen, Antiserum, Control 2 Autokit CH50
46 14987481164625 991-34891 991-34891 In-Vitro Diagnostic Use JLH Titrimetric, Fatty Acids 1 HR Series NEFA-HR(2) Color Reagent B
47 14987481164533 999-00404 999-00404 In-Vitro Diagnostic Use LBR Ldl & Vldl Precipitation, Hdl 1 L-Type LDL-C Reagent 1
48 14987481100999 276-76491 276-76491 In-Vitro Diagnostic Use JIT Calibrator, Secondary 2 NEFA Standard Solution
49 10856626006011 276-76491 276-76491 In-Vitro Diagnostic Use JIT Calibrator, Secondary NEFA Standard Solution
50 04987481164680 991-60301 991-60301 In-Vitro Diagnostic Use OUE Micro Total Analysis Instrument System 2 uTASWako i30
Other products with the same Product Code "LBR"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00657498000663 0599-020 0599-020 For Use in the Determination of High Density Lipoprotein (HDL) Cholesterol in Se For Use in the Determination of High Density Lipoprotein (HDL) Cholesterol in Serum or Plasma. HDL Cholesterol Precipitating Reagent STANBIO LABORATORY, L.P.
2 00628063400706 80-4607-00 80-4607-00 N-geneous LDL Cholesterol Reagent (R2) SEKISUI DIAGNOSTICS, LLC
3 00628063400690 80-4604-00 80-4604-00 N-geneous LDL Cholesterol Reagent (R1) SEKISUI DIAGNOSTICS, LLC
4 00628063400683 80-4601-00 80-4601-00 N-geneous LDL Cholesterol Reagent (R2) SEKISUI DIAGNOSTICS, LLC
5 00628063400676 80-4598-00 80-4598-00 N-geneous LDL Cholesterol Reagent (R1) SEKISUI DIAGNOSTICS, LLC
6 00628063400669 7120 7120 LDL Direct LS Cholesterol Reagent Kit SEKISUI DIAGNOSTICS, LLC
7 00381934750019 4750 4750 The CardioChek® Plus Home Self-Test analyzer is intended for self-testing in lay The CardioChek® Plus Home Self-Test analyzer is intended for self-testing in lay users. It is intended to be used by a single person and should not be shared. The CardioChek® Plus Home Self-Test analyzer is for in vitro diagnostic use to test whole blood from the fingertip. The specific analyte measured is determined by the type of test strip chosen. CardioChek Plus Home Self-Test Analyzer POLYMER TECHNOLOGY SYSTEMS, INC.
8 00381934722016 4722 4722 CardioChek® Plus Home Lipid Panel Self-Test test strips are in vitro diagnostic CardioChek® Plus Home Lipid Panel Self-Test test strips are in vitro diagnostic devices used to measure total cholesterol, HDL cholesterol, and triglycerides levels in human whole blood from the fingertip, as well as providing a calculated value for LDL levels. These test strips must be used in conjunction with a CardioChek® PA, CardioChek Plus or CardioChek Plus Home Self-Test analyzer. CardioChek Plus Home Lipid Panel Self-Test Strip 2ct POLYMER TECHNOLOGY SYSTEMS, INC.
9 00381934721019 4721 4721 CardioChek Plus Home Lipid + eGLU Smart Bundle Self-Test test strips are in vitr CardioChek Plus Home Lipid + eGLU Smart Bundle Self-Test test strips are in vitro diagnostic devices used to measure glucose and lipid (total cholesterol / HDL cholesterol / and triglyceride) levels in human whole blood from the fingertip. These test strips must be used in conjunction with a CardioChek Plus Home Self-Test analyzer. CardioChek Plus Home Lipid + eGLU Smart Bundle Self-Test 2ct POLYMER TECHNOLOGY SYSTEMS, INC.
10 00381934720012 4720 4720 The CardioChek® Plus Home Self-Test analyzer is intended for self-testing in lay The CardioChek® Plus Home Self-Test analyzer is intended for self-testing in lay users. It is intended to be used by a single person and should not be shared. The CardioChek® Plus Home Self-Test analyzer is for in vitro diagnostic use to test whole blood from the fingertip. The specific analyte measured is determined by the type of test strip chosen. CardioChek Plus Home Self-Test Analyzer POLYMER TECHNOLOGY SYSTEMS, INC.
11 00381932729017 2729 2729 CardioChek Plus Lipid + eGLU Test Strips Smart Bundle™ are in vitro diagnostic d CardioChek Plus Lipid + eGLU Test Strips Smart Bundle™ are in vitro diagnostic devices used to monitor glucose and lipid (total cholesterol / HDL cholesterol / and triglyceride) levels in human whole blood. These test strips must be used in conjunction with a CardioChek Plus analyzer. CardioChek Plus Lipid + eGLU Test Strips Smart Bundle™ (2-pk) POLYMER TECHNOLOGY SYSTEMS, INC.
12 00381932702010 2702 2702 The CardioChek® Plus professional analyzer is intended for in vitro diagnostic u The CardioChek® Plus professional analyzer is intended for in vitro diagnostic use to test whole blood. The specific analyte measured is determined by the type of test strip chosen. CardioChek® Plus Professional Analyzer, Refurbished POLYMER TECHNOLOGY SYSTEMS, INC.
13 00381932701013 2701 2701 The CardioChek® Plus professional analyzer is intended for in vitro diagnostic u The CardioChek® Plus professional analyzer is intended for in vitro diagnostic use to test whole blood. The specific analyte measured is determined by the type of test strip chosen. CardioChek® Plus Professional Analyzer POLYMER TECHNOLOGY SYSTEMS, INC.
14 00381932700016 2700 2700 The CardioChek® Plus professional analyzer is intended for in vitro diagnostic u The CardioChek® Plus professional analyzer is intended for in vitro diagnostic use to test whole blood. The specific analyte measured is determined by the type of test strip chosen. CardioChek® Plus Professional Analyzer POLYMER TECHNOLOGY SYSTEMS, INC.
15 00381932478014 2478 2478 CardioChek Plus Lipid + eGLU Test Strips Smart Bundle™ are in vitro diagnostic d CardioChek Plus Lipid + eGLU Test Strips Smart Bundle™ are in vitro diagnostic devices used to monitor glucose and lipid (total cholesterol / HDL cholesterol / and triglyceride) levels in human whole blood. These test strips must be used in conjunction with a CardioChek Plus analyzer. CardioChek Plus Lipid + eGLU Test Strips Smart Bundle™ (2-pk) POLYMER TECHNOLOGY SYSTEMS, INC.
16 00381932477017 2477 2477 PTS Panels® CHOL+HDL+GLU test strips are in vitro diagnostic devices used to mon PTS Panels® CHOL+HDL+GLU test strips are in vitro diagnostic devices used to monitor total cholesterol; HDL cholesterol; and glucose levels in human whole blood. These test strips must be used in conjunction with a CardioChek Plus or CardioChek PA analyzer. PTS Panels® CHOL+HDL+GLU Test Strips (10-ct ) + MEMoChip POLYMER TECHNOLOGY SYSTEMS, INC.
17 00381932470018 2470 2470 PTS Panels® Lipid Panel test strips are in vitro diagnostic devices used to moni PTS Panels® Lipid Panel test strips are in vitro diagnostic devices used to monitor total cholesterol, HDL cholesterol, and triglycerides levels in human whole blood, as well as providing a calculated value for LDL levels. These test strips must be used in conjunction with a CardioChek® PA or Plus analyzer. PTS Panels® Lipid Panel Test Strips (10-ct) POLYMER TECHNOLOGY SYSTEMS, INC.
18 00381932469012 2469 2469 PTS Panels® CHOL+HDL+GLU test strips are in vitro diagnostic devices used to mon PTS Panels® CHOL+HDL+GLU test strips are in vitro diagnostic devices used to monitor total cholesterol; HDL cholesterol; and glucose levels in human whole blood. These test strips must be used in conjunction with a CardioChek Plus or CardioChek PA analyzer. PTS Panels® CHOL+HDL+GLU Test Strips (10-ct ) POLYMER TECHNOLOGY SYSTEMS, INC.
19 00381932412018 2412 2412 PTS Panels® CHOL+HDL+GLU test strips are in vitro diagnostic devices used to mon PTS Panels® CHOL+HDL+GLU test strips are in vitro diagnostic devices used to monitor total cholesterol; HDL cholesterol; and glucose levels in human whole blood. These test strips must be used in conjunction with a CardioChek Plus or CardioChek PA analyzer. PTS Panels® CHOL+HDL+GLU Test Strips POLYMER TECHNOLOGY SYSTEMS, INC.
20 00381932400015 2400 2400 PTS Panels® Metabolic Chemistry test strips are in vitro diagnostic devices used PTS Panels® Metabolic Chemistry test strips are in vitro diagnostic devices used to monitor glucose; HDL cholesterol; and triglycerides levels in human whole blood. These test strips must be used in conjunction with a CardioChek Plus or CardioChek PA analyzer. PTS Panels® Metabolic ChemistryTest Strips POLYMER TECHNOLOGY SYSTEMS, INC.
21 00381931821019 1821 1821 PTS Panels CHOL+HDL test strips are in vitro diagnostic devices used to monitor PTS Panels CHOL+HDL test strips are in vitro diagnostic devices used to monitor HDL cholesterol and total cholesterol levels in human whole blood. These test strips must be used in conjunction with a CardioChek Plus or CardioChek PA analyzer. PTS Panels® CHOL+HDL Test Strips POLYMER TECHNOLOGY SYSTEMS, INC.
22 00381931788015 1788 1788 PTS Panels® HDL Cholesterol test strips are in vitro diagnostic devices used to PTS Panels® HDL Cholesterol test strips are in vitro diagnostic devices used to monitor HDL cholesterol levels in human whole blood. These test strips must be used in conjunction with a CardioChek® brand analyzer. PTS Panels® HDL Cholesterol Test Strips POLYMER TECHNOLOGY SYSTEMS, INC.
23 00381931782013 1782 1782 The CardioChek® analyzer is intended for in vitro diagnostic use to test whole b The CardioChek® analyzer is intended for in vitro diagnostic use to test whole blood. The specific analyte measured is determined by the type of test strip chosen. CardioChek® Analyzer; Refurbished POLYMER TECHNOLOGY SYSTEMS, INC.
24 00381931757011 1757 1757 The CardioChek® PA professional analyzer is intended for in vitro diagnostic use The CardioChek® PA professional analyzer is intended for in vitro diagnostic use to test whole blood. The specific analyte measured is determined by the type of test strip chosen. CardioChek® PA Professional Analyzer, Refurbished POLYMER TECHNOLOGY SYSTEMS, INC.
25 00381931714014 1714 1714 PTS Panels® HDL Cholesterol test strips are in vitro diagnostic devices used to PTS Panels® HDL Cholesterol test strips are in vitro diagnostic devices used to monitor HDL cholesterol levels in human whole blood. These test strips must be used in conjunction with a CardioChek® brand analyzer. PTS Panels® HDL Cholesterol Test Strips POLYMER TECHNOLOGY SYSTEMS, INC.
26 00381931710016 1710 1710 PTS Panels® Lipid Panel test strips are in vitro diagnostic devices used to moni PTS Panels® Lipid Panel test strips are in vitro diagnostic devices used to monitor total cholesterol, HDL cholesterol, and triglycerides levels in human whole blood, as well as providing a calculated value for LDL levels. These test strips must be used in conjunction with a CardioChek® PA or Plus analyzer. PTS Panels® Lipid Panel Test Strips POLYMER TECHNOLOGY SYSTEMS, INC.
27 00381931709010 1709 1709 The CardioChek® analyzer is intended for in vitro diagnostic use to test whole b The CardioChek® analyzer is intended for in vitro diagnostic use to test whole blood. The specific analyte measured is determined by the type of test strip chosen. CardioChek® analyzer POLYMER TECHNOLOGY SYSTEMS, INC.
28 00381931708013 1708 1708 The CardioChek® PA professional analyzer is intended for in vitro diagnostic use The CardioChek® PA professional analyzer is intended for in vitro diagnostic use to test whole blood. The specific analyte measured is determined by the type of test strip chosen. CardioChek® PA analyzer POLYMER TECHNOLOGY SYSTEMS, INC.
29 00381930860019 860 860 ChekMate™ Strips are dry strips that mimic the use of the PTS Panels test strips ChekMate™ Strips are dry strips that mimic the use of the PTS Panels test strips to check the CardioChek analyzer system optics, calibration, and result handling algorithms. ChekMate™ Strips POLYMER TECHNOLOGY SYSTEMS, INC.
30 00380740129972 07P7120 07P7120 Alinity c Direct LDL Reagent Kit Alinity ABBOTT LABORATORIES
31 00380740000356 1E31-20 01E3120 Direct LDL ARCHITECT ABBOTT LABORATORIES
32 00304040040539 5700534 5700534 CardioChek Plus Analyzer Starter Pack CardioChek HENRY SCHEIN, INC.
33 00304040037713 5700411 5700411 CardioChek Plus Analyzer CardioChek HENRY SCHEIN, INC.
34 14987481164595 993-72691 993-72691 In-Vitro Diagnostic Use L-Type HDL-C Reagent 2 FUJIFILM WAKO PURE CHEMICAL CORPORATION
35 14987481164588 997-72591 997-72591 In-Vitro Diagnostic Use L-Type HDL-C Reagent 1 FUJIFILM WAKO PURE CHEMICAL CORPORATION
36 14987481164540 999-00504 999-00504 In-Vitro Diagnostic Use L-Type LDL-C Reagent 2 FUJIFILM WAKO PURE CHEMICAL CORPORATION
37 14987481164533 999-00404 999-00404 In-Vitro Diagnostic Use L-Type LDL-C Reagent 1 FUJIFILM WAKO PURE CHEMICAL CORPORATION
38 10856626006196 997-72591 997-72591 In-Vitro Diagnostic Use L-Type HDL-C Reagent 1 FUJIFILM WAKO PURE CHEMICAL CORPORATION
39 10856626006097 993-72691 993-72691 In-Vitro Diagnostic Use L-Type HDL-C Reagent 2 FUJIFILM WAKO PURE CHEMICAL CORPORATION
40 10763924550507 MD550 Lipid and Glucose Measuring System LipidPlus® Meter JANT PHARMACAL CORPORATION
41 10758750009527 1669829 1669829 VITROS Chemistry Products CHOL Slides VITROS ORTHO-CLINICAL DIAGNOSTICS, INC.
42 10304040037741 5700414 5700414 CardioChek Lipid Panel Test CardioChek HENRY SCHEIN, INC.
43 10304040037734 5700412 5700412 CardioChek 15Lipid/15Glucose CardioChek HENRY SCHEIN, INC.
44 08809319396512 99LS10-2 CURO L7 Lipid Test Strip - Lipid Profile SD BIOSENSOR, INC.
45 08809319396161 99LA10G-2 CURO L7 Analyzer SD BIOSENSOR, INC.
46 07613336121375 08057966190 08057966190 LDL-Cholesterol Gen.3 ROCHE DIAGNOSTICS GMBH
47 05060500091996 IR059-1200 IR059-1200 LDL-Cholesterol Reagent 2 X 66 mL + 1 X 44 mL Synermed® INFRARED LABORATORY SYSTEMS LLC
48 05060500090869 IR059-WK IR059-WK LDL-Cholesterol Reagent 1 X 25 mL + 1 X 8.4 mL Synermed® INFRARED LABORATORY SYSTEMS LLC
49 05060500090852 IR059-X IR059-X LDL-Cholesterol Reagent 1 X 60 mL + 1 X 20 mL Synermed® INFRARED LABORATORY SYSTEMS LLC
50 05060500090845 IR059-R IR059-R LDL-Cholesterol Reagent 1 X 240 mL + 1 X 80 mL Synermed® INFRARED LABORATORY SYSTEMS LLC