Other products from "SYSMEX CORPORATION"
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
Other products with the same Product Codes "JPA, GKP"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00850044118052 ICO-3000 iHealth IHEALTH LAB INC.
2 00850044118045 ICO-3000 iHealth IHEALTH LAB INC.
3 00842768026812 10487098 ORKL19 Standard Human Plasma for the calibration of coagulation and fibrinolysis tests Standard Human Plasma SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
4 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
5 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
6 00842768014444 10446524 OVIP15 The BCS Cuvette Rotor is part of the BCS-XP system. BCS® System Cuvette Rotors SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
7 00842768014222 10446232 ORHO37 Supplementary Reagent for coagulation tests Calcium Chloride Solution SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
8 00842768012358 10446541 OVMN11 The cuvettes serve coagulation tests as a reaction vessel. Cuvettes for BFT // Analyzer SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
9 00842768012259 10446530 OVKG03 The cuvettes serve coagulation tests as a reaction vessel. BFT II Analyzer Dispo System SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
10 00842768012198 10446526 OVIS31 Behring Coagulation Cup serves as vessel for samples, human plasma and buffer solutions. Behring Coagulation Cup SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
11 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
12 00842768006869 10445989 OPCC03 For calibration of the Berichrom Heparin assay for measurement of unfractionated heparin Berichrom® Heparin UF Calibrator SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
13 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
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15 00817869020274 SC-127 SC-127 Whole Blood Control Level III ANALYTICAL CONTROL SYSTEMS INC
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20 00630414945514 10459330 OVOB03 The Behring Coagulation System (BCS XP System) performs quantitative assays of s The Behring Coagulation System (BCS XP System) performs quantitative assays of specific parameters in human citrated plasma BCS® XP System SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
21 00613994615633 313-51 DEVICE 313-51 HEPTRAC ELEC QLT CNTRL CEM HEPtrac® MEDTRONIC, INC.
22 B55890013181 900-1318 900-1318 The Reference Plasma Quality Control Kit is for use with the Sonoclot® Analyzer The Reference Plasma Quality Control Kit is for use with the Sonoclot® Analyzer System to verify performance of activated cuvettes. Testing should be performed prior to the use of a new shipment of activated cuvettes and monthly throughout use of the stock. More frequent testing may be required to comply with local, state and federal QC requirements. Reference plasma quality control is important to properly verify proper performance of coagulation test activators. A two level testing approach is used to perform quality control of the activator used in an activated coagulation test. Level I is run with the activator on the reference plasma. Level II is run with the non-activated test on the reference plasma. These two tests confirm the effectiveness of the activator to perform its intended coagulation activation.Each Kit contains:1 vial Reference Plasma Control - 6 ml vial containing a lyophilized preparation of citrated animal plasma, stabilizers and buffer. Contains no human material.1 vial Distilled Water - 6 ml vial containing 5.0 ml laboratory grade distilled water.1 vial 0.02 M Calcium Chloride - 6 ml vial containing 5.0 ml 0.02 M Calcium Chloride.5 plastic 1 ml syringes2 non-activated test cuvettes (blue with clear caps, stir bars, and probes) Sonoclot® Reference Plasma Quality Control Kit SIENCO, INC.
23 B55890013021 900-1302 900-1302 The Reference Viscosity Oil QC test is a simple means of verifying proper operat The Reference Viscosity Oil QC test is a simple means of verifying proper operation of the Sonoclot Analyzer. This test consists of a two point verification of the electromechanical oscillator and also ensures that the heating control is operating accurately. The two verification points are: 1) Probe-In-Air, and 2) Probe-In-Oil. The Probe-In-Air is the response of the electromechanical oscillator to air. The Probe-In-Oil is the response of the electromechanical oscillator to the reference viscosity liquid. Since the viscosity of the reference viscosity fluid is significantly temperature dependent, the Probe-In-Oil test point also verifies the temperature regulation. The QC test should be run each day the Sonoclot Analyzer is used or as required by your institution. Each Reference Viscosity Quality Control Kit contains 24 cuvettes, 24 probes, 1 vial of reference viscosity oil with end cap, and these instructions. These supplies provide 24 QC tests for the analyzer. Sonoclot® Reference Viscosity Oil Quality Control Kit SIENCO, INC.
24 B55880004321 800-0432 800-0432 The SonACT Kit is an in vitro diagnostic reagent for use with the Sonoclot® Coag The SonACT Kit is an in vitro diagnostic reagent for use with the Sonoclot® Coagulation & Platelet Function Analyzer System. The SonACT test is a celite activated whole blood clotting time test. It may also be used with citrated whole blood and plasma. The SonACT Kit is intended for general purpose global hemostasis monitoring including: clot detection, fibrin formation, platelet function, and hyperfibrinolysis. The monitoring information is typically used for anticoagulant management up to high heparin levels (0 to approximately 6 units per ml), hypercoagulable and/or hypocoagulable screening, platelet function assessment, and hyperfibrinolysis screening. When used with the Sonoclot Analyzer System, the SonACT test provides quantitative Onset/ACT and Clot Rate results as well as qualitative and quantitative information on the Sonoclot Signature including: fibrin formation, platelet function, and hyperfibrinolysis.Each kit contains 100 lidded colorless plastic activation cuvettes, 100 probes, and instructions for use. The activation cuvettes contain a controlled amount of celite and a magnetic stir bar. Sonoclot® SonACT Kit SIENCO, INC.
25 B55880004311 800-0431 800-0431 The SonACT Kit is an in vitro diagnostic reagent for use with the Sonoclot® Coag The SonACT Kit is an in vitro diagnostic reagent for use with the Sonoclot® Coagulation & Platelet Function Analyzer System. The SonACT test is a celite activated whole blood clotting time test. It may also be used with citrated whole blood and plasma. The SonACT Kit is intended for general purpose global hemostasis monitoring including: clot detection, fibrin formation, platelet function, and hyperfibrinolysis. The monitoring information is typically used for anticoagulant management up to high heparin levels (0 to approximately 6 units per ml), hypercoagulable and/or hypocoagulable screening, platelet function assessment, and hyperfibrinolysis screening. When used with the Sonoclot Analyzer System, the SonACT test provides quantitative Onset/ACT and Clot Rate results as well as qualitative and quantitative information on the Sonoclot Signature including: fibrin formation, platelet function, and hyperfibrinolysis.Each kit contains 24 lidded colorless plastic activation cuvettes, 24 probes, and instructions for use. The activation cuvettes contain a controlled amount of celite and a magnetic stir bar. Sonoclot® SonACT Kit SIENCO, INC.
26 B55880004261 800-0426 800-0426 The Non-Activated Clotting Test Kit contains the necessary components for an in The Non-Activated Clotting Test Kit contains the necessary components for an in vitro diagnostic test for use with the Sonoclot® Coagulation & Platelet Function Analyzer System. It may be used with native whole blood, citrated whole blood, and plasma. The Non-Activated Kit may either be used as a non-activated clotting test or as a general use test with user provided activators. It is intended for customer designed hemostasis monitoring on the Sonoclot Analyzer. The Non-Activated cuvette allows for coagulation monitoring using tissue activation, thrombin activation, and other custom activators. Some of the applications for the Non-Activated test with the addition of customer determined reagents are monitoring of fibrin formation, fibrinolysis, hyperfibrinolysis and clot retraction. When used with the Sonoclot Analyzer System, the Non-Activated test provides quantitative Onset/ACT and Clot Rate results as well as qualitative and quantitative information on the Sonoclot Signature including: fibrin formation, platelet function, and hyperfibrinolysis. Each kit contains 24 lidded plastic cuvettes, 24 probes, and instructions for use. The cuvettes contain a magnetic stir bar. Sonoclot® NonActivated Kit SIENCO, INC.
27 B55880004251 800-0425 800-0425 The Non-Activated Clotting Test Kit contains the necessary components for an in The Non-Activated Clotting Test Kit contains the necessary components for an in vitro diagnostic test for use with the Sonoclot® Coagulation & Platelet Function Analyzer System. It may be used with native whole blood, citrated whole blood, and plasma. The Non-Activated Kit may either be used as a non-activated clotting test or as a general use test with user provided activators. It is intended for customer designed hemostasis monitoring on the Sonoclot Analyzer. The Non-Activated cuvette allows for coagulation monitoring using tissue activation, thrombin activation, and other custom activators. Some of the applications for the Non-Activated test with the addition of customer determined reagents are monitoring of fibrin formation, fibrinolysis, hyperfibrinolysis and clot retraction. When used with the Sonoclot Analyzer System, the Non-Activated test provides quantitative Onset/ACT and Clot Rate results as well as qualitative and quantitative information on the Sonoclot Signature including: fibrin formation, platelet function, and hyperfibrinolysis. Each kit contains 100 lidded plastic cuvettes, 100 probes, and instructions for use. The cuvettes contain a magnetic stir bar. Sonoclot® NonActivated Kit SIENCO, INC.
28 B55880004011 800-0401 800-0401 The kACT Kit is an in vitro diagnostic test for use with the Sonoclot® Coagulat The kACT Kit is an in vitro diagnostic test for use with the Sonoclot® Coagulation & Platelet Function Analyzer System. The kACT test is a kaolin activated whole blood clotting time test. It may also be used with citrated whole blood and plasma. The kACT Kit is intended for high dose heparin management with or without aprotinin. The kACT test provides quantitative Onset/ACT and Clot Rate results with the Sonoclot Analyzer. The kACT test is not intended for platelet function monitoring. Each kit contains 24 lidded blue plastic activation cuvettes, 24 probes, and instructions for use. The activation cuvettes contain a controlled amount of kaolin and a magnetic stir bar. Sonoclot® kACT Kit SIENCO, INC.
29 B55880004001 800-0400 800-0400 The kACT Kit is an in vitro diagnostic test for use with the Sonoclot Coagulatio The kACT Kit is an in vitro diagnostic test for use with the Sonoclot Coagulation & Platelet Function Analyzer System. The kACT test is a kaolin activated whole blood clotting time test. It may also be used with citrated whole blood and plasma.The kACT kit is intended for high dose heparin management with or without aprotinin. The kACT test provides quantitative Onset/ACT and Clot Rate results with the Sonoclot Analyzer. The kACT test is not intended for platelet function monitoring.Each kACT Kit contains 100 lidded blue plastic activation cuvettes, 100 probes, and instructions for use. The activation cuvettes contain a controlled amount of kaolin and a magnetic stir bar. Sonoclot® kACT Kit SIENCO, INC.
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