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 14987481164564 991-00101 991-00101 In-Vitro Diagnostic Use JIS Calibrator, Primary 2 L-Type HDL-C Reagent 1
11 14987481164540 999-00504 999-00504 In-Vitro Diagnostic Use LBR Ldl & Vldl Precipitation, Hdl 1 L-Type LDL-C Reagent 2
12 10856626006196 997-72591 997-72591 In-Vitro Diagnostic Use LBR Ldl & Vldl Precipitation, Hdl L-Type HDL-C Reagent 1
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 00860394001256 CURO L5 Total Cholesterol Strips Total Cholesterol Strips CURO L5 Total Cholesterol Strips KPI HEALTHCARE, INC.
2 00860394001225 CURO L5 CURO L5 CURO L5 Cholesterol and Glucose measuring system CURO L5 KPI HEALTHCARE, INC.
3 00852169008201 LDL1230 LDL1230 In Vitro Diagnostics testing kit R1:3X45mL, R2:3X15mL ClearChem Diagnostics Inc. Low-Density Lipoprotein (LDL) Cholesterol CLEARCHEM DIAGNOSTICS INC.
4 00850006113064 Curo L5 CURO L5 Glucose Strip Curo L5 KPI HEALTHCARE, INC.
5 00817439021151 HDL505 HDL505 For the quantitative determination high-density lipoprotein cholesterol in human For the quantitative determination high-density lipoprotein cholesterol in human serum or plasma using the Polychem 180 analyzer. For in vitro diagnostic use only. 3 x 51 ml, 2 x 20 ml MedTest DX autoHDL for PC180 MEDTEST DX, INC.
6 00817439020888 HDLC480 HDLC480 auto HDL/LDL Calibrator, For the calibration of autoHDL™ and autoLDL™ Cholestero auto HDL/LDL Calibrator, For the calibration of autoHDL™ and autoLDL™ Cholesterol Reagent Set in serum or plasma. For in vitro diagnostic use only. Size: 3 x 40mL, 3 x 14mL MedTest DX auto HDL/LDL Calibrator MEDTEST DX, INC.
7 00817439020871 HDL600 HDL600 HDL600, for the quantitative determination high-density lipoprotein cholesterol HDL600, for the quantitative determination high-density lipoprotein cholesterol in human serum or plasma using the Mindray BS-200 analyzer. For in vitro diagnostic use only. Size: 3 x 51 ml, 2 x 20 ml MedTest DX autoHDL / BS200 MEDTEST DX, INC.
8 00817439020864 HDL480 HDL480 AutoHDL™, For the quantitative determination high-density lipoprotein cholestero AutoHDL™, For the quantitative determination high-density lipoprotein cholesterol in human serum or plasma using the Mindray BS-480 analyzer. For in vitro diagnostic use only. Size: 4 x 57 ml, 4 x 18 ml. MedTest DX autoHD™L / BS480 MEDTEST DX, INC.
9 00817302023060 DT616 DT616 HDLD (HDL Cholesterol Direct) w/ calibrator 4 x 250 tests CAROLINA LIQUID CHEMISTRIES CORP.® HDLD REAGENT PRODUCT NO. DT616 CAROLINA LIQUID CHEMISTRIES CORPORATION
10 00817302022667 CC667 CC667 LDLD (LDL Cholesterol Direct) w/ cal 2 x 200 tests CAROLINA LIQUID CHEMISTRIES CORP.® LDL DIRECT REAGENT CC667 CAROLINA LIQUID CHEMISTRIES CORPORATION
11 00817302022216 CC615 CC615 HDLD W/CALIBRATOR, 2 X 200 tests CAROLINA LIQUID CHEMISTRIES CORP.® HDL DIRECT CC615 CAROLINA LIQUID CHEMISTRIES CORPORATION
12 00817302022209 AU-616 AU-616 HDLD (High Density Lipoprotein Direct) w/ cal 3 x 250 tests CAROLINA LIQUID CHEMISTRIES CORP.® HDLD RGT. KIT AU-616 CAROLINA LIQUID CHEMISTRIES CORPORATION
13 00817302022193 BL616 BL616 HDLD (High Density Lipoprotein Direct) w/ cal 3 x 100 tests CAROLINA LIQUID CHEMISTRIES CORP.® HDL RGT. KIT BL-616 CAROLINA LIQUID CHEMISTRIES CORPORATION
14 00817302022186 ST616 ST616 HDLD (HDL Cholesterol Direct) w/ cal 2 x 250 tests CAROLINA LIQUID CHEMISTRIES CORP.® CLC720 HDL RGT KIT Product No. ST616 CAROLINA LIQUID CHEMISTRIES CORPORATION
15 00812137012074 R1 x 2 x 70mL, R2 x 1 x 50mL 501-420 The LDL-Cholesterol Reagent Set is intended for the in vitro quantitative determ The LDL-Cholesterol Reagent Set is intended for the in vitro quantitative determination of Low Density Lipoprotein Cholesterol in human serum or plasma. The reagents can assist in the diagnosis and treatment of patients at risk of developing coronary heart disease. Elevated LDL cholesterol is the primary target of cholesterol-lowering therapy. LDL Cholesterol Reagent Set CLINICAL DIAGNOSTIC SOLUTIONS, INC.
16 00811727016171 16-H7545-320 16-H7545-320 Pointe autoHDL Cholesterol Reagent packaged for use on the Mindray BA800. 4 x 60 Pointe autoHDL Cholesterol Reagent packaged for use on the Mindray BA800. 4 x 60ml R1, 4 x 20ml R2. For the quantitative determination high-density lipoprotein cholesterol in human serum or plasma using the Mindray BA-800M analyzer. For in vitro diagnostic use only. Rx Only. Pointe autoHDL Cholesterol Reagent POINTE SCIENTIFIC, INC.
17 00811727015860 14-H7545-300 14-H7545-400 Pointe autoHDL Reagent packaged for use on the BS480 Analyzer. 4x57mL, 4x18mL Ki Pointe autoHDL Reagent packaged for use on the BS480 Analyzer. 4x57mL, 4x18mL Kit. For the quantitative determination high-density lipoprotein cholesterol in human serum or plasma. For in vitro diagnostic use only. Pointe autoHDL for the BS480 POINTE SCIENTIFIC, INC.
18 00811727015051 OH945-480 OH945-480 Pointe Scientific, Inc. autoHDL Cholesterol Reagent is for the quantitative dete Pointe Scientific, Inc. autoHDL Cholesterol Reagent is for the quantitative determination high-density lipoprotein cholesterol in human serum or plasma. For in vitro diagnostic use only. Packaged for use on Olympus Analyzers. 6 x 60ml, 6 x 20ml Pointe Scientific, Inc. autoHDL Cholesterol POINTE SCIENTIFIC, INC.
19 00811727014306 13-H7512-STD 13-H7512-STD HDL Cholesterol Standard, for use as a cholesterol standard for standardization HDL Cholesterol Standard, for use as a cholesterol standard for standardization or calibration of enzymatic, endpoint cholesterol assays used with HDL Cholesterol procedures.Size: 1 x 15 mL. Concentration: 50 mg/dL Pointe Scientific, Inc. POINTE SCIENTIFIC, INC.
20 00811727014290 13-H7511-30 13-H7511-30 HDL Reagent, for the quantitative determination of High Density Lipoprotein (HDL HDL Reagent, for the quantitative determination of High Density Lipoprotein (HDL) in Cholesterol in serum. Size: 1 x 30 mL Pointe Scientific, Inc. POINTE SCIENTIFIC, INC.
21 00811727013552 12-H7545-162 12-H7545-162 For the quantitative determination high-density lipoprotein cholesterol in human For the quantitative determination high-density lipoprotein cholesterol in human serum or plasma. For in vitro diagnostic use only. autoHDL POINTE SCIENTIFIC, INC.
22 00811727012913 HH945-480 HH945-480 HDL reagent for the quantitative determination high-density lipoprotein choleste HDL reagent for the quantitative determination high-density lipoprotein cholesterol in human serum or plasma. For in vitro diagnostic use only.6 x 60ml, 6 x 20ml Pointe Scientific POINTE SCIENTIFIC, INC.
23 00811727012807 HH945-240 HH945-240 autoHDL Cholesterol Reagent, for the quantitative determination high-density lip autoHDL Cholesterol Reagent, for the quantitative determination high-density lipoprotein cholesterol in human serum or plasma. For in vitro diagnostic use only. Size: 6 x 30mL, 3 x 20mL Pointe Scientific, Inc. POINTE SCIENTIFIC, INC.
24 00811727011459 H7512-STD H7512-STD Reagent intended for use as an cholesterol standard for standardization or calib Reagent intended for use as an cholesterol standard for standardization or calibration of enzymatic, endpoint cholesterol assays used with HDL Cholesterol procedures1 x 15ml Pointe Scientific, Inc. POINTE SCIENTIFIC, INC.
25 00811727011442 H7511-60 H7511-60 Reagent for the quantitative determination of High Density Lipoprotein (HDL) in Reagent for the quantitative determination of High Density Lipoprotein (HDL) in Cholesterol in serum.2 x 30ml Pointe Scientific, Inc. POINTE SCIENTIFIC, INC.
26 00811727011435 H7507-80 H7507-80 Reagent for the quantitative determination of High Density Lipoprotein (HDL) in Reagent for the quantitative determination of High Density Lipoprotein (HDL) in serum.8 x 10ml Pointe Scientific, Inc. POINTE SCIENTIFIC, INC.
27 00811727011411 H7545-CAL H7545-CAL Reagent for the calibration of Pointe Scientific’s autoHDL and autoLDL Cholester Reagent for the calibration of Pointe Scientific’s autoHDL and autoLDL Cholesterol Reagent Set in serum or plasma. For in vitro diagnostic use only.1 x 3ml Pointe Scientific, Inc. POINTE SCIENTIFIC, INC.
28 00811727011404 H7545-1000 H7545-1000 Reagent for the quantitative determination high-density lipoprotein cholesterol Reagent for the quantitative determination high-density lipoprotein cholesterol in human serum or plasma. For in vitro diagnostic use only.1 x 750ml, 1 x 250ml Pointe Scientific, Inc. POINTE SCIENTIFIC, INC.
29 00811727011398 H7545-320 H7545-320 Reagent for the quantitative determination high-density lipoprotein cholesterol Reagent for the quantitative determination high-density lipoprotein cholesterol in human serum or plasma. For in vitro diagnostic use only.1 x 240ml, 1 x 80ml Pointe Scientific, Inc. POINTE SCIENTIFIC, INC.
30 00811727011381 H7545-80 H7545-80 Reagent for the quantitative determination high-density lipoprotein cholesterol Reagent for the quantitative determination high-density lipoprotein cholesterol in human serum or plasma. For in vitro diagnostic use only.1 x 60ml, 1 x 20ml Pointe Scientific, Inc. POINTE SCIENTIFIC, INC.
31 00811727011374 H7545-40 H7545-40 Reagent for the quantitative determination high-density lipoprotein cholesterol Reagent for the quantitative determination high-density lipoprotein cholesterol in human serum or plasma. For in vitro diagnostic use only.1 x 30ml, 1 x 10ml Pointe Scientific, Inc. POINTE SCIENTIFIC, INC.
32 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.
33 00628063400706 80-4607-00 80-4607-00 N-geneous LDL Cholesterol Reagent (R2) SEKISUI DIAGNOSTICS, LLC
34 00628063400690 80-4604-00 80-4604-00 N-geneous LDL Cholesterol Reagent (R1) SEKISUI DIAGNOSTICS, LLC
35 00628063400683 80-4601-00 80-4601-00 N-geneous LDL Cholesterol Reagent (R2) SEKISUI DIAGNOSTICS, LLC
36 00628063400676 80-4598-00 80-4598-00 N-geneous LDL Cholesterol Reagent (R1) SEKISUI DIAGNOSTICS, LLC
37 00628063400669 7120 7120 LDL Direct LS Cholesterol Reagent Kit SEKISUI DIAGNOSTICS, LLC
38 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.
39 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.
40 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.
41 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.
42 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.
43 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.
44 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.
45 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.
46 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.
47 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.
48 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.
49 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.
50 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.