No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 04987562433698 | CN383000 | UF-CALIBRATOR | JIW | Calibrator, surrogate | UF-CALIBRATOR | ||
2 | 14987562460332 | 213528 | XN CAL 5X3.0ML | KRX | CALIBRATOR FOR CELL INDICES | 2 | XN CAL | |
3 | 04987562444779 | CJ445012 | Fully Automated Urine Particle Digital Imaging Device UD-10 | JOY | DEVICE, AUTOMATED CELL-LOCATING | 2 | Fully Automated Urine Particle Digital Imaging Device UD-10 | |
4 | 04987562434572 | BD634545 | Automated Hematology Analyzer XN-L series XN-550 | GKZ | Counter, differential cell | 2 | Automated Hematology Analyzer XN-L series XN-550 | |
5 | 04987562425716 | CK978289 | Automated Blood Coagulation Analyzer CA-660 | GKP | INSTRUMENT, COAGULATION, AUTOMATED | 2 | Automated Blood Coagulation Analyzer CA-600 series CA-660 | |
6 | 04987562425426 | BY990757 | CS-5100 COMPLETE | JPA | SYSTEM, MULTIPURPOSE FOR IN VITRO COAGULATION STUDIES | 2 | Automated Blood Coagulation Analyzer CS-5100 | |
7 | 04987562408535 | 06404310 | UF ll CALIBRATOR | JIW | CALIBRATOR, SURROGATE | UF ll CALIBRATOR | ||
8 | 14987562460387 | 218981 | Range Check X lll 24X3.0ML WBC/RBC/PLT | JPK | MIXTURE, HEMATOLOGY QUALITY CONTROL | 2 | RANGE CHECK X lll | |
9 | 14987562508003 | CC118360 | Platelet CHECK | Platelet CHECK Level 2-16x3.0ML | GJP | Control, Platelet | 2 | Platelet CHECK |
10 | 14987562507990 | CN464998 | Platelet CHECK | Platelet CHECK Level 1-16x3.0ML | GJP | Control, Platelet | 2 | Platelet CHECK |
11 | 04987562440139 | BN344411 | Fully Automated Urine Particle Analyzer UF-5000 | LKM | COUNTER, URINE PARTICLE | 2 | Fully Automated Urine Particle Analyzer UF-5000 | |
12 | 04987562434534 | AW618382 | Automated Hematology Analyzer XN-L series XN-350 | GKZ | Counter, differential cell | 2 | Automated Hematology Analyzer XN-L series XN-350 | |
13 | 04987562429219 | AR408878 | Automated Hematology Analyzer XP-300 | GKZ,GKL | Counter, differential cell,COUNTER, CELL, AUTOMATED (PARTICLE COUNTER) | 2 | Automated Hematology Analyzer XP series XP-300 | |
14 | 04987562412860 | BB046392 | XS-1000iC Complete | GKZ | Counter, differential cell | 2 | Automated Hematology Analyzer XS series XS-1000iC | |
15 | 14987562460578 | 199-5002-0 | E-Check (XS) 5X1.5MLX2 Normal/High | GLQ,JPK | MIXTURE, CONTROL, WHITE-CELL AND RED-CELL INDICES,MIXTURE, HEMATOLOGY QUALITY CONTROL | 2 | e-CHECK(XS) | |
16 | 14987562460561 | 199-5001-0 | E-Check (XS) 5X1.5MLX1 Low | JPK,GLQ | MIXTURE, HEMATOLOGY QUALITY CONTROL,MIXTURE, CONTROL, WHITE-CELL AND RED-CELL INDICES | 2 | e-CHECK(XS) | |
17 | 04987562434527 | CX851950 | Automated Hematology Analyzer XN-L series XN-330 | GKZ | Counter, differential cell | 2 | Automated Hematology Analyzer XN-L series XN-330 | |
18 | 04987562433735 | BV981798 | CS-2500 COMPLETE | JPA | SYSTEM, MULTIPURPOSE FOR IN VITRO COAGULATION STUDIES | 2 | Automated Blood Coagulation Analyzer CS-2500 | |
19 | 14987562460356 | 213537 | XN CAL PF 5X3.0ML | KRX | CALIBRATOR FOR CELL INDICES | 2 | XN CAL PF | |
20 | 04987562424214 | AP795756 | XN-10 Complete | GKZ | Counter, differential cell | 2 | Automated Hematology Analyzer XN series XN-10 | |
21 | 14987562460349 | 213536 | XN CAL PF 1X3.0ML | KRX | CALIBRATOR FOR CELL INDICES | 2 | XN CAL PF | |
22 | 04987562434541 | CL032175 | Automated Hematology Analyzer XN-L series XN-430 | GKZ | Counter, differential cell | 2 | Automated Hematology Analyzer XN-L series XN-430 | |
23 | 04987562432615 | CS297931 | XN-11 Complete | GKZ | Counter, differential cell | 2 | Automated Hematology Analyzer XN series XN-11 | |
24 | 04987562424221 | AE797961 | Automated Hematology Analyzer XN series XN-20 | GKZ | Counter, differential cell | 2 | Automated Hematology Analyzer XN series XN-20 | |
25 | 04987562408542 | 05366719 | Sysmex UF-1000i™ Automated Urine Particle Analyzer | LKM | COUNTER, URINE PARTICLE | 2 | Fully Automated Urine Particle Analyzer UF-1000i | |
26 | 04987562406807 | 05342311 | Sysmex XS-1000i™ Automated Hematology Analyzer | GKZ | Counter, differential cell | 2 | Automated Hematology Analyzer XS series XS-1000i | |
27 | 14987562460615 | 200-4004-1 | plt-CHECK Level 2- 12X4.5ML | JPK | MIXTURE, HEMATOLOGY QUALITY CONTROL | 2 | plt-CHECK | |
28 | 14987562460608 | 200-4004-0 | plt-CHECK Level 1-12X4.5ML | JPK | MIXTURE, HEMATOLOGY QUALITY CONTROL | 2 | plt-CHECK | |
29 | 14987562460592 | 110-4008-0 | X-Cal FSR Kit (5X4.6ML) | KRX | CALIBRATOR FOR CELL INDICES | 2 | X-CAL Calibrator | |
30 | 14987562460585 | 110-4009-0 | X-Cal Hematology Calibrator (4.6ML) | KRX | CALIBRATOR FOR CELL INDICES | 2 | X-CAL Calibrator | |
31 | 14987562460394 | AS747750 | XN-L CHECK | JPK | MIXTURE, HEMATOLOGY QUALITY CONTROL | 2 | XN-L CHECK | |
32 | 14987562460288 | 199-4004-1 | E-Check 4X4.5MLX3 Low/Normal/High | JPK,GLQ | MIXTURE, HEMATOLOGY QUALITY CONTROL,MIXTURE, CONTROL, WHITE-CELL AND RED-CELL INDICES | 2 | e-CHECK | |
33 | 04987562434565 | BQ391107 | Automated Hematology Analyzer XN-L series XN-530 | GKZ | Counter, differential cell | 2 | Automated Hematology Analyzer XN-L series XN-530 | |
34 | 04987562490110 | CT129514 | Automated Hematology Analyzer XW-100 | GKZ | Counter, differential cell | 2 | Automated Hematology Analyzer XW-100 | |
35 | 04987562434558 | BM392756 | Automated Hematology Analyzer XN-L series XN-450 | GKZ | Counter, differential cell | 2 | Automated Hematology Analyzer XN-L series XN-450 | |
36 | 04987562402021 | 02318618 | pocH-100i (US) | GKZ,GKL | Counter, differential cell,COUNTER, CELL, AUTOMATED (PARTICLE COUNTER) | 2 | Automated Hematology Analyzer pocH-100i | |
37 | 14987562460325 | 213527 | XN CAL 1X3.0ML | KRX | CALIBRATOR FOR CELL INDICES | 2 | XN CAL | |
38 | 14987562460318 | 213516 | XN CHECK BF 6X3.0ML L 1,2 | JPK | MIXTURE, HEMATOLOGY QUALITY CONTROL | 2 | XN CHECK BF | |
39 | 14987562460370 | 217685 | SCS-1000 Universal Calibrator 1X2ML | KSA | CALIBRATOR FOR RED-CELL AND WHITE-CELL COUNTING | 2 | SCS-1000 Calibrator | |
40 | 14987562461797 | AX844619 | WRP CHECK EX | JPK | MIXTURE, HEMATOLOGY QUALITY CONTROL | 2 | WRP CHECK EX | |
41 | 14987562460257 | 130-4003-0 | Range Check X ll | JPK | MIXTURE, HEMATOLOGY QUALITY CONTROL | 2 | RANGE CHECK X ll | |
42 | 04987562404087 | 03309313 | Automated Hematology Analyzer XE-2100D | GKZ | Counter, differential cell | 2 | Automated Hematology Analyzer XE-2100D | |
43 | 14987562502766 | NSH-100G | BV166979 | XN CHECK 8 x 3.0mL, Level 3 | JPK | Mixture, Hematology Quality Control | 2 | XN CHECK |
44 | 14987562502759 | NSN-100G | CV649926 | XN CHECK 8 x 3.0mL, Level 2 | JPK | Mixture, Hematology Quality Control | 2 | XN CHECK |
45 | 14987562502742 | NSL-100G | AF640985 | XN CHECK 8 x 3.0mL, Level 1 | JPK | Mixture, Hematology Quality Control | 2 | XN CHECK |
46 | 14987562490216 | BP935764 | XW QC CHECK | JPK | Mixture, hematology quality control | 2 | XW QC CHECK | |
47 | 14987562461780 | BG234784 | WRP CHECK | JPK | MIXTURE, HEMATOLOGY QUALITY CONTROL | 2 | WRP CHECK | |
48 | 14987562460295 | 201-6001-0 | E-Check (XE) 4X4.5MLX3 Levels | JPK | MIXTURE, HEMATOLOGY QUALITY CONTROL | 2 | e-CHECK(XE) | |
49 | 14987562460264 | 140-3004-0 | EightCheck-3WP X-tra 4X2MLX3 Lo/Norm/Hi | JPK | MIXTURE, HEMATOLOGY QUALITY CONTROL | 2 | EIGHTCHECK-3WP | |
50 | 04987562409471 | 06372511 | CS-2100i COMPLETE | JPA | SYSTEM, MULTIPURPOSE FOR IN VITRO COAGULATION STUDIES | 2 | Automated Blood Coagulation Analyzer CS-2100i |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 05391521421081 | M01000 | Destiny MAX Analyzer | TCOAG IRELAND LIMITED | ||
2 | 05391521421029 | H01000P | Destiny Plus | TCOAG IRELAND LIMITED | ||
3 | 05391521421012 | N04000 | KC® 4 Delta | TCOAG IRELAND LIMITED | ||
4 | 05391521421005 | G05000 | KC® 1 Delta | TCOAG IRELAND LIMITED | ||
5 | 04987562433735 | BV981798 | CS-2500 COMPLETE | Automated Blood Coagulation Analyzer CS-2500 | SYSMEX CORPORATION | |
6 | 04987562425716 | CK978289 | Automated Blood Coagulation Analyzer CA-660 | Automated Blood Coagulation Analyzer CA-600 series CA-660 | SYSMEX CORPORATION | |
7 | 04987562425686 | BR142626 | Automated Blood Coagulation Analyzer CA-620 | Automated Blood Coagulation Analyzer CA-600 series CA-620 | SYSMEX CORPORATION | |
8 | 04987562425686 | BR142626 | Automated Blood Coagulation Analyzer CA-620 | Automated Blood Coagulation Analyzer CA-600 series CA-620 | SYSMEX CORPORATION | |
9 | 04987562425426 | BY990757 | CS-5100 COMPLETE | Automated Blood Coagulation Analyzer CS-5100 | SYSMEX CORPORATION | |
10 | 04987562409471 | 06372511 | CS-2100i COMPLETE | Automated Blood Coagulation Analyzer CS-2100i | SYSMEX CORPORATION | |
11 | 04987562205936 | 01412714 | CA CAL S 3.0X3 (GCL-100A) | CA CAL S | SYSMEX CORPORATION | |
12 | G0561025161 | 102516 | 102516 | Lupus Anticoagulant Confirmation Reagent | BIO/DATA CORPORATION | |
13 | 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 |
14 | 04260160470372 | sigma | 211000 | The ROTEM sigma is an in vitro diagnostic (IVD) whole blood hemostasis system in The ROTEM sigma is an in vitro diagnostic (IVD) whole blood hemostasis system intended for use in the evaluation of coagulopathies in Point of Care (POC) or laboratory settings. It uses rotational thromboelastometry to provide semiquantitative information about the coagulation state of a blood sample. The ROTEM sigma system records the kinetic changes in a sample of 3.2% citrated whole blood during clot formation, as well as when the sample clot retracts and/or lyses.Several parameters are measured and reported for this purpose. The graphical presentation reflects the various physiological results, which describe the interaction between coagulation factors and inhibitors, fibrinogen, platelets, and the fibrinolysis system. Additionally, the effect of certain drugs influencing hemostasis, in particular some anticoagulants (e.g. heparin), can be detected. | ROTEM® | TEM INNOVATIONS GMBH |
15 | 04260160470358 | sigma ROTROL P | 555202 | The ROTEM sigma is an in vitro diagnostic (IVD) whole blood hemostasis system in The ROTEM sigma is an in vitro diagnostic (IVD) whole blood hemostasis system intended for use in the evaluation of coagulopathies in Point of Care (POC) or laboratory settings. It uses rotational thromboelastometry to provide semiquantitative information about the coagulation state of a blood sample. The ROTEM sigma system records the kinetic changes in a sample of 3.2% citrated whole blood during clot formation, as well as when the sample clot retracts and/or lyses.Several parameters are measured and reported for this purpose. The graphical presentation reflects the various physiological results, which describe the interaction between coagulation factors and inhibitors, fibrinogen, platelets, and the fibrinolysis system. Additionally, the effect of certain drugs influencing hemostasis, in particular some anticoagulants (e.g. heparin), can be detected. | ROTEM® | TEM INNOVATIONS GMBH |
16 | 04260160470341 | sigma ROTROL N | 555201 | The ROTEM sigma is an in vitro diagnostic (IVD) whole blood hemostasis system in The ROTEM sigma is an in vitro diagnostic (IVD) whole blood hemostasis system intended for use in the evaluation of coagulopathies in Point of Care (POC) or laboratory settings. It uses rotational thromboelastometry to provide semiquantitative information about the coagulation state of a blood sample. The ROTEM sigma system records the kinetic changes in a sample of 3.2% citrated whole blood during clot formation, as well as when the sample clot retracts and/or lyses.Several parameters are measured and reported for this purpose. The graphical presentation reflects the various physiological results, which describe the interaction between coagulation factors and inhibitors, fibrinogen, platelets, and the fibrinolysis system. Additionally, the effect of certain drugs influencing hemostasis, in particular some anticoagulants (e.g. heparin), can be detected. | ROTEM® | TEM INNOVATIONS GMBH |
17 | 04260160470327 | sigma complete + hep | 555502 | The ROTEM sigma is an in vitro diagnostic (IVD) whole blood hemostasis system in The ROTEM sigma is an in vitro diagnostic (IVD) whole blood hemostasis system intended for use in the evaluation of coagulopathies in Point of Care (POC) or laboratory settings. It uses rotational thromboelastometry to provide semiquantitative information about the coagulation state of a blood sample. The ROTEM sigma system records the kinetic changes in a sample of 3.2% citrated whole blood during clot formation, as well as when the sample clot retracts and/or lyses.Several parameters are measured and reported for this purpose. The graphical presentation reflects the various physiological results, which describe the interaction between coagulation factors and inhibitors, fibrinogen, platelets, and the fibrinolysis system. Additionally, the effect of certain drugs influencing hemostasis, in particular some anticoagulants (e.g. heparin), can be detected. | ROTEM® | TEM INNOVATIONS GMBH |
18 | 04260160470242 | ex-tem® | 503-05-US | The EXTEM assay is a semi-quantitative in vitro diagnostic assay used to monitor The EXTEM assay is a semi-quantitative in vitro diagnostic assay used to monitor the coagulation process via the extrinsic 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)). CFT and alpha (Speed of Clot Formation) are complementary parameters and should be used in conjunction with the main parameters Clotting Time (CT) and Clot Firmness (A20/MCF). | ROTEM® | TEM INNOVATIONS GMBH |
19 | 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 |
20 | 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 |
21 | 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 |
22 | 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 |
23 | 04260160470075 | fib-tem® | 503-06-US | The FIBTEM assay is a semi-quantitative in vitro diagnostic assay on the ROTEM® The FIBTEM assay is a semi-quantitative in vitro diagnostic assay on the ROTEM® delta Thromboelastometry System to monitor the clot firmness of citrated whole blood specimens after blocking platelet contribution to the clot firmness. fib-tem® is always used in conjunction with ex-tem®. Clotting characteristics are described by the functional parameter Clot Firmness (A20/MCF). | ROTEM® | TEM INNOVATIONS GMBH |
24 | 04260160470068 | ap-tem® | 503-04-US | The APTEM assay is a semi-quantitative in vitro diagnostic assay on the ROTEM® d The APTEM assay is a semi-quantitative in vitro diagnostic assay on the ROTEM® delta Thromboelastometry System to monitor the clot firmness of citrated whole blood specimens after blocking hyperfibrinolysis by aprotinin. ap-tem® is always used in conjunction with ex-tem®. 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)). CFT and alpha (Speed of Clot Formation) are complementary parameters and should be used in conjunction with the main parameters Clotting Time (CT) and Clot Firmness (A20/MCF). | ROTEM® | TEM INNOVATIONS GMBH |
25 | 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 |
26 | 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 |
27 | 03607450590272 | 59027 | STA R Max® (with cap piercing option) | DIAGNOSTICA STAGO | ||
28 | 03607450590265 | 59026 | STA R Max® | DIAGNOSTICA STAGO | ||
29 | 03607450590135 | 59013 | STA R Max® | DIAGNOSTICA STAGO | ||
30 | 03607450590104 | 59010 | STA R Max® (with cap piercing option) | DIAGNOSTICA STAGO | ||
31 | 03607450589900 | 58990 | STA Compact Max® | DIAGNOSTICA STAGO | ||
32 | 03607450589894 | 58989 | STA Compact Max® (with cap piercing option) | DIAGNOSTICA STAGO | ||
33 | 03607450589795 | 58979 | STA-R Evolution® Expert Series (with cap piercing option) | DIAGNOSTICA STAGO | ||
34 | 03607450589788 | 58978 | STA-R Evolution® Expert Series | DIAGNOSTICA STAGO | ||
35 | 03607450582307 | 58230 | ST art® | DIAGNOSTICA STAGO | ||
36 | 03607450581041 | 58104 | STA Satellite® | DIAGNOSTICA STAGO | ||
37 | 00850044118052 | ICO-3000 | iHealth | IHEALTH LAB INC. | ||
38 | 00850044118045 | ICO-3000 | iHealth | IHEALTH LAB INC. | ||
39 | 00842768026812 | 10487098 | ORKL19 | Standard Human Plasma for the calibration of coagulation and fibrinolysis tests | Standard Human Plasma | SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH |
40 | 00842768024887 | 10458677 | OVKF032 | The BFT II Analyzer is a semi-automated device intended for use to determine PT, The BFT II Analyzer is a semi-automated device intended for use to determine PT, APTT and Fibrinogen | BFT II Analyzer | SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH |
41 | 00842768017742 | 10446684 | OWZC39 | Washing Solution is used for cleaning the Siemens Healthcare Diagnostics coagula Washing Solution is used for cleaning the Siemens Healthcare Diagnostics coagulation analyzers | Washing Solution for Coagulation Analyzers | SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH |
42 | 00842768014444 | 10446524 | OVIP15 | The BCS Cuvette Rotor is part of the BCS-XP system. | BCS® System Cuvette Rotors | SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH |
43 | 00842768014222 | 10446232 | ORHO37 | Supplementary Reagent for coagulation tests | Calcium Chloride Solution | SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH |
44 | 00842768012358 | 10446541 | OVMN11 | The cuvettes serve coagulation tests as a reaction vessel. | Cuvettes for BFT // Analyzer | SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH |
45 | 00842768012259 | 10446530 | OVKG03 | The cuvettes serve coagulation tests as a reaction vessel. | BFT II Analyzer Dispo System | SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH |
46 | 00842768012198 | 10446526 | OVIS31 | Behring Coagulation Cup serves as vessel for samples, human plasma and buffer solutions. | Behring Coagulation Cup | SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH |
47 | 00842768008023 | 10446125 | OQSC11 | Check of the proper functioning and precision of the pipettors on the BCS® Syste Check of the proper functioning and precision of the pipettors on the BCS® System, the BCS® XP System and the BCT System | BC Validation Kit | SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH |
48 | 00842768006869 | 10445989 | OPCC03 | For calibration of the Berichrom Heparin assay for measurement of unfractionated heparin | Berichrom® Heparin UF Calibrator | SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH |
49 | 00842768006845 | 10445987 | OPCA03 | For calibration of the Berichrom Heparin assay for measurement of low molecular For calibration of the Berichrom Heparin assay for measurement of low molecular weight heparin | Berichrom® Heparin LMW Calibrator | SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH |
50 | 00817869020311 | SC-125, SC-126, H2O | Hemotec Whole Blood Control Kit Large | ANALYTICAL CONTROL SYSTEMS INC |