Other products from "HYPHEN BIOMED"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 03663537008184 221003 221003 KFF Assay, Heparin 2 BIOPHEN HEPARIN 3
2 03663537008474 AR002A AR002A Calcium chloride 0.25M (M/4)
3 03663537084782 AR001L AR001L Calcium chloride 0.025M (M/40)
4 03663537084768 AR001B AR001B Calcium chloride 0.025M (M/40)
5 03663537046803 RK041A RK041A LCO Platelet Factor 4 Radioimmunoassay 2 ZYMUTEST HIA MonoStrip IgG
6 03663537008467 AR001K Calcium chloride 0.025M (M/40)
7 03663537008450 AR001A AR001A Calcium chloride 0.025M (M/40)
8 03663537008313 223301 223301 GGN Plasma, Coagulation Control 2 BIOPHEN ABNORMAL CONTROL PLASMA
9 03663537043512 224401 224401 GGN Plasma, Coagulation Control 2 BIOPHEN LMWH CONTROL LOW CII
10 03663537008283 223001 223001 GGN Plasma, Coagulation Control 2 BIOPHEN LMWH Control Plasma
11 03663537007989 223801 223801 GGN Plasma, Coagulation Control 2 BIOPHEN LMWH Control C3
12 03663537010446 AR021L AR021L Imidazole buffer
13 03663537010439 AR021K AR021K Imidazole buffer
14 03663537084843 AR021N Imidazole buffer
15 03663537084829 AR021M Imidazole buffer
16 03663537084805 AR021B Imidazole buffer
17 03663537008290 223101 223101 GGN Plasma, Coagulation Control 2 BIOPHEN UFH Control Plasma
18 03663537008047 AR021A AR021A Imidazole buffer
19 03663537043550 224201 224201 GGN Plasma, Coagulation Control 2 BIOPHEN LMWH Control C4
20 03663537043505 224301 224301 GGN Plasma, Coagulation Control 2 BIOPHEN LMWH CONTROL LOW CI
21 03663537042904 224101 224101 GGN Plasma, Coagulation Control 2 BIOPHEN UFH Control C1
22 03663537008306 223201 223201 GGN Plasma, Coagulation Control 2 BIOPHEN NORMAL CONTROL PLASMA
23 03663537008191 221006 221006 KFF Assay, Heparin 2 BIOPHEN HEPARIN 6
24 03663537046810 RK041D RK041D LCO Platelet Factor 4 Radioimmunoassay 2 ZYMUTEST HIA MonoStrip IgGAM
25 03663537008320 223405 223405 GGN Plasma, Coagulation Control 2 BIOPHEN™ V-L Control Plasma
26 03663537008238 221205 221205 GGP Test, Qualitative And Quantitative Factor Deficiency 2 BIOPHEN Protein C 5
27 03663537018763 RK040A RK040A LCO Platelet Factor 4 Radioimmunoassay 2 ZYMUTEST HIA IgG
28 03663537019074 222401 222401 JIT Calibrator, Secondary 2 BIOPHEN™ V-L Plasma Calibrator
29 03663537018770 RK040D RK040D LCO Platelet Factor 4 Radioimmunoassay 2 ZYMUTEST HIA IgGAM
30 03663537008214 221105 221105 JBQ Antithrombin Iii Quantitation 2 BIOPHEN Antithrombin 5
31 03663537008207 221102 221102 JBQ Antithrombin Iii Quantitation 2 BIOPHEN Antithrombin 2.5
32 03663537008368 223701 223701 GGN Plasma, Coagulation Control 2 BIOPHEN LMWH Control Low
33 03663537008276 222301 222301 GGN Plasma, Coagulation Control 2 BIOPHEN UFH Calibrator
34 03663537008245 222001 222001 GGN Plasma, Coagulation Control 2 BIOPHEN Heparin Calibrator
35 03663537017964 CK065K CK065K GGW Test, Time, Partial Thromboplastin 2 HEMOCLOT Quanti. V-L
36 03663537008481 AR002K AR002K Calcium chloride 0.25M (M/4)
37 03663537008221 221202 221202 GGP Test, Qualitative And Quantitative Factor Deficiency 2 BIOPHEN Protein C 2.5
38 03663537007996 223901 223901 GGN Plasma, Coagulation Control 2 BIOPHEN UFH CONTROL C2
Other products with the same Product Code "GGN"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 04260160470587 delta System (US/CA) 201001 The ROTEM® delta is designed for in-vitro diagnostic use by professionals in a l The ROTEM® delta is designed for in-vitro diagnostic use by professionals in a laboratory environment. The ROTEM® delta is intended to be used to provide a qualitative and quantitative indication of the coagulation state of a blood sample. For this purpose the ROTEM® delta records the clot firmness changes in a sample of citrated whole blood as the sample clots, retracts and lyses in real time. The analyzer output consists of a qualitative graphical representation (mirrored coagulation curve - clot firmness over time) and several defined numerical parameters describing the curve quantitatively. ROTEM® TEM INNOVATIONS GMBH
2 04260160470112 ROTROL P 503-25-US, 503-25 ROTROL P is a quality control material for monitoring accuracy and precision of ROTROL P is a quality control material for monitoring accuracy and precision of tests carried out on the ROTEM® delta Thromboelastometry System. For in vitro diagnostic use only. ROTEM® TEM INNOVATIONS GMBH
3 04260160470105 ROTROL N 503-24-US, 503-24 ROTROL N is a quality control material for monitoring accuracy and precision of ROTROL N is a quality control material for monitoring accuracy and precision of tests carried out on the ROTEM® delta Thromboelastometry System. For in vitro diagnostic use only. ROTEM® TEM INNOVATIONS GMBH
4 04260160470099 star-tem® 20 503-10-US The ROTEM® delta is designed for in-vitro diagnostic use by professionals in a l The ROTEM® delta is designed for in-vitro diagnostic use by professionals in a laboratory environ-ment. The ROTEM® delta is intended to be used to provide a qualitative and quantitative indication of the coagulation state of a blood sample. For this purpose the ROTEM® delta records the clot firmness changes in a sample of citrated whole blood as the sample clots, retracts and lyses in real time. The analyzer output consists of a qualitative graphical representation (mirrored coagulation curve – clot firmness over time) and several defined numerical parameters describing the curve quantitatively.The star-tem® reagent is intended for use as recalcification reagent in the NATEM and INTEM assay on the ROTEM® delta. The corresponding assays are described in the NATEM assay application sheet and in the Instructions for Use of the in-tem® reagent (REF 503-02-US), resp. ROTEM® TEM INNOVATIONS GMBH
5 04260160470082 hep-tem® 503-09-US The ROTEM® delta is designed for in-vitro diagnostic use by professionals in a l The ROTEM® delta is designed for in-vitro diagnostic use by professionals in a laboratory environ-ment. The ROTEM® delta is intended to be used to provide a qualitative and quantitative indication of the coagulation state of a blood sample. For this purpose the ROTEM® delta records the clot firmness changes in a sample of citrated whole blood as the sample clots, retracts and lyses in real time. The analyzer output consists of a qualitative graphical representation (mirrored coagulation curve - clot firmness over time) and several defined numerical parameters describing the curve quantitatively.The hep-tem® assay is a semi-quantitative in vitro diagnostic assay used to inactivate heparin in patients receiving unfractionated heparin on the ROTEM® delta. To monitor the coagulation process citrated whole blood specimens are used. Clotting characteristics are described by the functional parameters Clotting Time (CT), Speed of Clot Formation (CFT and alpha angle), Clot Firmness (A20/MCF) and Clot Lysis (LOT, ML, LI(x)). ROTEM® TEM INNOVATIONS GMBH
6 04260160470044 in-tem® 503-02-US The ROTEM® delta is designed for in-vitro diagnostic use by professionals in a l The ROTEM® delta is designed for in-vitro diagnostic use by professionals in a laboratory environment. The ROTEM® delta is intended to be used to provide a qualitative and quantitative indication of the coagulation state of a blood sample. For this purpose the ROTEM® delta records the clot firmness changes in a sample of citrated whole blood as the sample clots, retracts and lyses in real time. The analyzer output consists of a qualitative graphical representation (mirrored coagulation curve - clot firmness over time) and several defined numerical parameters describing the curve quantitatively.The in-tem® assay is a semi-quantitative in vitro diagnostic assay used to monitor the coagulation process via the intrinsic pathway in citrated whole blood specimens on the ROTEM® delta. Clotting characteristics are described by the functional parameters Clotting Time (CT), Speed of Clot Formation (CFT and alpha angle), Clot Firmness (A20/MCF) and Clot Lysis (LOT, ML, LI(x)). ROTEM® TEM INNOVATIONS GMBH
7 04260160470020 delta System 200100-US The ROTEM® delta is designed for in-vitro diagnostic use by professionals in a l The ROTEM® delta is designed for in-vitro diagnostic use by professionals in a laboratory environment. The ROTEM® delta is intended to be used to provide a qualitative and quantitative indication of the coagulation state of a blood sample. For this purpose the ROTEM® delta records the clot firmness changes in a sample of citrated whole blood as the sample clots, retracts and lyses in real time. The analyzer output consists of a qualitative graphical representation (mirrored coagulation curve - clot firmness over time) and several defined numerical parameters describing the curve quantitatively. ROTEM® TEM INNOVATIONS GMBH
8 03663537043550 224201 224201 BIOPHEN LMWH Control C4 HYPHEN BIOMED
9 03663537043512 224401 224401 BIOPHEN LMWH CONTROL LOW CII HYPHEN BIOMED
10 03663537043505 224301 224301 BIOPHEN LMWH CONTROL LOW CI HYPHEN BIOMED
11 03663537042904 224101 224101 BIOPHEN UFH Control C1 HYPHEN BIOMED
12 03663537008368 223701 223701 BIOPHEN LMWH Control Low HYPHEN BIOMED
13 03663537008320 223405 223405 BIOPHEN™ V-L Control Plasma HYPHEN BIOMED
14 03663537008313 223301 223301 BIOPHEN ABNORMAL CONTROL PLASMA HYPHEN BIOMED
15 03663537008306 223201 223201 BIOPHEN NORMAL CONTROL PLASMA HYPHEN BIOMED
16 03663537008290 223101 223101 BIOPHEN UFH Control Plasma HYPHEN BIOMED
17 03663537008283 223001 223001 BIOPHEN LMWH Control Plasma HYPHEN BIOMED
18 03663537008276 222301 222301 BIOPHEN UFH Calibrator HYPHEN BIOMED
19 03663537008252 222101 222101 BIOPHEN PLASMA CALIBRATOR HYPHEN BIOMED
20 03663537008245 222001 222001 BIOPHEN Heparin Calibrator HYPHEN BIOMED
21 03663537007996 223901 223901 BIOPHEN UFH CONTROL C2 HYPHEN BIOMED
22 03663537007989 223801 223801 BIOPHEN LMWH Control C3 HYPHEN BIOMED
23 03607450006865 00686 STA® - Quality HBPM/LMWH DIAGNOSTICA STAGO
24 03607450006780 00678 STA® - System Control N + P DIAGNOSTICA STAGO
25 03607450006773 00677 STA® - Coag Control (N + ABN) PLUS DIAGNOSTICA STAGO
26 03607450006766 00676 STA® - Coag Control N + ABN DIAGNOSTICA STAGO
27 03607450005264 00526 STA® - Liatest® Control N + P DIAGNOSTICA STAGO
28 03607450003819 00381 STA® - Quality HNF/UFH DIAGNOSTICA STAGO
29 03607450002010 00201 STA® - Control LA 1 + 2 DIAGNOSTICA STAGO
30 00885074184937 550-11 CALCIUM CHLORIDE 5 ML NA MEDTRONIC, INC.
31 00859110005111 903se 903se Validate Heparin is intended for the quantitative determination of Calibration V Validate Heparin is intended for the quantitative determination of Calibration Verification/Linearity of the heparin anti-Xa activity on automated instruments Validate LGC CLINICAL DIAGNOSTICS, INC.
32 00859110005104 903st 903st Validate Heparin is intended for the quantitative determination of Calibration V Validate Heparin is intended for the quantitative determination of Calibration Verification/Linearity of the heparin anti-Xa activityon automated instruments Validate LGC CLINICAL DIAGNOSTICS, INC.
33 00859110005098 903il 903il Validate Heparin is intended for the quantitative determination of Calibration V Validate Heparin is intended for the quantitative determination of Calibration Verification/Linearity of the heparin anti-Xa activityon automated instruments Validate LGC CLINICAL DIAGNOSTICS, INC.
34 00859110005081 902se 902se Validate D-Dimer is intended for the quantitative determination of Calibration V Validate D-Dimer is intended for the quantitative determination of Calibration Verification/Linearity of drug analytes on automated instruments. Validate LGC CLINICAL DIAGNOSTICS, INC.
35 00859110005074 902st 902st Validate D-Dimer is intended for the quantitative determination of Calibration V Validate D-Dimer is intended for the quantitative determination of Calibration Verification/Linearity of drug analytes on automated instruments. Validate LGC CLINICAL DIAGNOSTICS, INC.
36 00859110005067 902il 902il Validate D-Dimer is intended for the quantitative determination of Calibration V Validate D-Dimer is intended for the quantitative determination of Calibration Verification/Linearity of drug analytes on automated instruments. Validate LGC CLINICAL DIAGNOSTICS, INC.
37 00850201006208 840C 840C ACTICLOT Protein C Resistance control plasmas BIOMEDICA ADI INC.
38 00847661004516 27102X 27102X Liquichek D-dimer Control MiniPak (A processed human plasma assayed D-dimer control.) Liquichek BIO-RAD LABORATORIES, INC.
39 00847661004509 27103 27103 Liquichek D-dimer Control Level 3 (A processed human plasma assayed D-dimer control.) Liquichek BIO-RAD LABORATORIES, INC.
40 00847661004493 27102 27102 Liquichek D-dimer Control Level 2 (A processed human plasma assayed D-dimer control.) Liquichek BIO-RAD LABORATORIES, INC.
41 00847661004486 27101 27101 Liquichek D-dimer Control Level 1 (A processed human plasma assayed D-dimer control.) Liquichek BIO-RAD LABORATORIES, INC.
42 00847661004479 27100 27100 Liquichek D-dimer Control Level Low (A processed human plasma assayed D-dimer control.) Liquichek BIO-RAD LABORATORIES, INC.
43 00847661001959 745X 745X Lyphochek Coagulation Control Level Trilevel MiniPak (A human plasma coagulatio Lyphochek Coagulation Control Level Trilevel MiniPak (A human plasma coagulation control.) Lyphochek BIO-RAD LABORATORIES, INC.
44 00847661001898 598X 598X Lyphochek Hemostasis Control MiniPak (A human plasma hemostasis control.) Lyphochek BIO-RAD LABORATORIES, INC.
45 00847661001041 599 599 Lyphochek Hemostasis Control Level 3 (A human plasma hemostasis control.) Lyphochek BIO-RAD LABORATORIES, INC.
46 00847661001034 598 598 Lyphochek Hemostasis Control Level 2 (A human plasma hemostasis control.) Lyphochek BIO-RAD LABORATORIES, INC.
47 00847661001027 597 597 Lyphochek Hemostasis Control Level 1 (A human plasma hemostasis control.) Lyphochek BIO-RAD LABORATORIES, INC.
48 00847661000792 746 746 Lyphochek Coagulation Control Level 3 (A human plasma coagulation control.) Lyphochek BIO-RAD LABORATORIES, INC.
49 00847661000785 745 745 Lyphochek Coagulation Control Level 2 (A human plasma coagulation control.) Lyphochek BIO-RAD LABORATORIES, INC.
50 00847661000778 744 744 Lyphochek Coagulation Control Level 1 (A human plasma coagulation control.) Lyphochek BIO-RAD LABORATORIES, INC.