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 10856626006196 997-72591 997-72591 In-Vitro Diagnostic Use LBR Ldl & Vldl Precipitation, Hdl L-Type HDL-C Reagent 1
14 04987481164529 995-06101 995-06101 In-Vitro Diagnostic Use JJX Single (Specified) Analyte Controls (Assayed And Unassayed) 1 Autokit Micro Albumin Calibrator Set
15 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
16 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
17 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)
18 04987481164666 999-06001 999-06001 In-Vitro Diagnostic Use JIQ Turbidimetric Method, Protein Or Albumin (Urinary, Non-Quant.) 1 Autokit Micro Albumin
19 00856626006168 997-60901 997-60901 In-Vitro Diagnostic Use JIT Calibrator, Secondary 2 uTASWako AFP-L3 Calibrator Set
20 00856626006120 995-60701 995-60701 In-Vitro Diagnostic Use OAU Des-Gamma-Carboxy-Prothrombin (Dcp), Risk Assessment, Hepatocellular Carcinoma 2 uTASWako DCP
21 14987481164618 995-34791 995-34791 In-Vitro Diagnostic Use JLH Titrimetric, Fatty Acids 1 HR Series NEFA-HR(2) Solvent A
22 14987481164496 991-61401 991-61401 In-Vitro Diagnostic Use JJX Single (Specified) Analyte Controls (Assayed And Unassayed) 1 uTASWako DCP Control H
23 10856626006066 991-61401 991-61401 In-Vitro Diagnostic Use JJX Single (Specified) Analyte Controls (Assayed And Unassayed) uTASWako DCP Control H
24 04987481164437 997-60901 997-60901 In-Vitro Diagnostic Use JIT Calibrator, Secondary 2 uTASWako AFP-L3 Calibrator Set
25 04987481164413 995-60701 995-60701 In-Vitro Diagnostic Use OAU Des-Gamma-Carboxy-Prothrombin (Dcp), Risk Assessment, Hepatocellular Carcinoma 2 uTASWako DCP
26 14987481164632 993-35191 993-35191 In-Vitro Diagnostic Use JLH Titrimetric, Fatty Acids 1 HR Series NEFA-HR(2) Solvent B
27 14987481164489 995-61301 995-61301 In-Vitro Diagnostic Use JJX Single (Specified) Analyte Controls (Assayed And Unassayed) 1 uTASWako DCP Control L
28 14987481164458 993-61101 993-61101 In-Vitro Diagnostic Use JJX Single (Specified) Analyte Controls (Assayed And Unassayed) 1 uTASWako AFP-L3 Control H
29 10856626006134 995-61301 995-61301 In-Vitro Diagnostic Use JJX Single (Specified) Analyte Controls (Assayed And Unassayed) uTASWako DCP Control L
30 10856626006073 993-61101 993-61101 In-Vitro Diagnostic Use JJX Single (Specified) Analyte Controls (Assayed And Unassayed) uTASWako AFP-L3 Control H
31 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
32 14987481164601 999-34691 999-34691 In-Vitro Diagnostic Use JLH Titrimetric, Fatty Acids 1 HR Series NEFA-HR(2) Color Reagent A
33 14987481164557 990-28011 990-28011 In-Vitro Diagnostic Use JIS Calibrator, Primary 2 HDL-C/LDL-C Calibrator
34 14987481164441 997-61001 997-61001 In-Vitro Diagnostic Use JJX Single (Specified) Analyte Controls (Assayed And Unassayed) 1 uTASWako AFP-L3 Control L
35 14987481102924 464-01601 464-01601 In-Vitro Diagnostic Use JIX Calibrator, Multi-Analyte Mixture 2 Multi Calibrator Lipids
36 10856626006172 997-61001 997-61001 In-Vitro Diagnostic Use JJX Single (Specified) Analyte Controls (Assayed And Unassayed) uTASWako AFP-L3 Control L
37 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)
38 10856626006035 990-28011 990-28011 In-Vitro Diagnostic Use JIS Calibrator, Primary HDL-C/LDL-C Calibrator
39 10856626006028 464-01601 464-01601 In-Vitro Diagnostic Use JIX Calibrator, Multi-Analyte Mixture Multi Calibrator Lipids
40 04987481164642 997-76491 997-76491 In-Vitro Diagnostic Use JJX Single (Specified) Analyte Controls (Assayed And Unassayed) 1 NEFA Linearity Material
41 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
42 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
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 "NSF"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 14987481164502 991-60801 991-60801 In-Vitro Diagnostic Use uTASWako Wash Solution FUJIFILM WAKO PURE CHEMICAL CORPORATION
2 14987481164465 997-61501 997-61501 In-Vitro Diagnostic Use uTASWako AFP-L3 Sample Dilution Buffer FUJIFILM WAKO PURE CHEMICAL CORPORATION
3 14987481164427 993-61601 993-61601 The uTASWako chip cassette is designed to be used for the assays on the uTASWako i30. uTASWako Chip Cassette FUJIFILM WAKO PURE CHEMICAL CORPORATION
4 10856626006189 997-61501 997-61501 In-Vitro Diagnostic Use uTASWako AFP-L3 Sample Dilution Buffer FUJIFILM WAKO PURE CHEMICAL CORPORATION
5 10856626006080 993-61601 993-61601 The uTASWako chip cassette is designed to be used for the assays on the uTASWako i30. uTASWako Chip Cassette FUJIFILM WAKO PURE CHEMICAL CORPORATION
6 10856626006059 991-60801 991-60801 In-Vitro Diagnostic Use uTASWako Wash Solution FUJIFILM WAKO PURE CHEMICAL CORPORATION
7 04987481164390 999-60601 999-60601 In-Vitro Diagnostic Use uTASWako AFP-L3 FUJIFILM WAKO PURE CHEMICAL CORPORATION
8 00856626006205 999-60601 999-60601 In-Vitro Diagnostic Use uTASWako AFP-L3 FUJIFILM WAKO PURE CHEMICAL CORPORATION