Other products from "MEDTRONIC, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00763000500993 BB11N31R1 CUSTOM PACK BB11N31R1 RESEARCH PACK DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
2 00763000500979 BB11N23R CUSTOM PACK BB11N23R 10PK XTRASUC DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
3 00763000500962 BB10R11R5 CUSTOM PACK BB10R11R5 PUMP PK DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
4 00763000500948 BB5Z34R5 CUSTOM PACK BB5Z34R5 NURSES DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
5 00763000500931 BB11G46R1 CUSTOM PACK BB11G46R1 RQST2 DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
6 00763000500634 7H97R2 CUSTOM PACK 7H97R2 25PK FEMALE ADAPT DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
7 00763000500559 HY10Z01R8 CUSTOM PACK HY10Z01R8 SUPPORT PACK DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
8 00763000501105 BB5B82R2 CUSTOM PACK BB5B82R2 5PK SUPPLE 2 DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
9 00763000511555 ONYXNG35012UX STENT ONYXNG35012UX ONYX 3.50X12RX NIQ Coronary drug-eluting stent 3 Onyx Frontier™
10 00763000498535 BB11L44R2 CUSTOM PACK BB11L44R2 OPEN HEART DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
11 00763000511470 ONYXNG30015UX STENT ONYXNG30015UX ONYX 3.00X15RX NIQ Coronary drug-eluting stent 3 Onyx Frontier™
12 00763000511418 ONYXNG27526UX STENT ONYXNG27526UX ONYX 2.75X26RX NIQ Coronary drug-eluting stent 3 Onyx Frontier™
13 00763000511326 ONYXNG25026UX STENT ONYXNG25026UX ONYX 2.50X26RX NIQ Coronary drug-eluting stent 3 Onyx Frontier™
14 00763000489472 HY7Y30R18 CUSTOM PACK HY7Y30R18 EC AMBU DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
15 00763000489434 BB7L75R3 CUSTOM PACK BB7L75R3 10PK 3/8X 72 DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
16 00763000426422 B3301533M LEAD B3301533M SENSIGHT 1.5MM EMAN LJ53 MHY,MRU,NHL,PJS,MBX Stimulator, electrical, implanted, for parkinsonian tremor,implanted subcortical Stimulator, electrical, implanted, for parkinsonian tremor,implanted subcortical electrical Stimulator (motor disorders),Stimulator, electrical, implanted, for parkinsonian symptoms,Stimulator, electrical, implanted, for essential tremor,Stimulator, thalamic, epilepsy, implanted 3 SenSight™
17 00763000426408 B3300542M LEAD B3300542M SENSIGHT 0.5MM EMAN LJ53 MBX,NHL,MRU,PJS,MHY Stimulator, thalamic, epilepsy, implanted,Stimulator, electrical, implanted, for Stimulator, thalamic, epilepsy, implanted,Stimulator, electrical, implanted, for parkinsonian symptoms,implanted subcortical electrical Stimulator (motor disorders),Stimulator, electrical, implanted, for essential tremor,Stimulator, electrical, implanted, for parkinsonian tremor 3 SenSight™
18 00763000334178 11D35R CUSTOM PACK 11D35R RETO5 DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
19 00763000334130 11D33R CUSTOM PACK 11D33R RETO1 DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
20 00763000306144 ETBF3216C166E STENT GRAFT ETBF3216C166E ENDUR II BIF MIH SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT 3 Endurant® II
21 00763000305659 ETLW1624C93E STENT GRAFT ETLW1624C93E ENDUR II LIMB MIH SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT 3 Endurant® II
22 00763000305598 ETLW1620C82E STENT GRAFT ETLW1620C82E ENDUR II LIMB MIH SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT 3 Endurant® II
23 00763000271220 7800RR36 RING 7800RR36 SIMUFORM SR 36MM US KRH RING, ANNULOPLASTY 2 SimuForm™
24 00763000271107 7700FR32 RING 7700FR32 SIMUPLUS FLEX 32MM US KRH RING, ANNULOPLASTY 2 SimuPlus™
25 00763000499945 BB5U74R18 CUSTOM PACK BB5U74R18 TUBING DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
26 00763000499921 BB8S37R29 CUSTOM PACK BB8S37R29 PUMP TBL DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
27 00763000511647 ONYXNG40012UX STENT ONYXNG40012UX ONYX 4.00X12RX NIQ Coronary drug-eluting stent 3 Onyx Frontier™
28 00763000498870 CB11N89R CUSTOM PACK CB11N89R MAN/BRIDGE DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
29 00763000260743 VNMC2828C90TU STENT GRAFT VNMC2828C90TU VAL NAV CS MIH SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT 3 Valiant Navion™
30 00763000001377 BB8B73R7 CUSTOM PACK BB8B73R7 PK DWE TUBING, PUMP, CARDIOPULMONARY BYPASS 2 NA
31 00681490024273 05328 CABLE 05328 ATAKR EGM SAFETY 8FT LPB Cardiac ablation percutaneous catheter 3 NA
32 00673978549071 5344 PLUG 5344 1/4 INCH DWE TUBING, PUMP, CARDIOPULMONARY BYPASS 2 NA
33 00643169796454 AB9U20100090 STENT AB9U20100090 ABRE V01 QAN Stent, iliac vein 3 Abre™
34 00643169518919 97740 PROG 97740 PATIENT MRICS SCS USA ROHS LGW STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF 3 NA
35 00643169078024 500FA27 MHV 500FA27 STD AORTIC LWQ HEART-VALVE, MECHANICAL 3 Open Pivot™
36 00613994759221 680R32 RING 680R32 PROFILE 3D 26L MEXICO KRH RING, ANNULOPLASTY 2 PROFILE 3D®
37 00613994691392 37642 PRGMR 37642 PATIENT DBS W SC,PC,RC MFR,NHL,MHY,OLM,MRU Stimulator, brain, implanted, for behavior modification,STIMULATOR, ELECTRICAL, Stimulator, brain, implanted, for behavior modification,STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN SYMPTOMS,STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR,Deep brain stimulator for obsessive compulsive disorder (OCD),implanted subcortical electrical Stimulator (motor disorders) 3 NA
38 00613994334565 68005YN CABLE 68005YN EGM 18L OCL Surgical Device, For cutting, coagulation, and/or ablation of tissue, including Surgical Device, For cutting, coagulation, and/or ablation of tissue, including cardiac tissue 2 NA
39 00885074469669 365538 TUNNEL TOOL 365538 ACCESSORY KIT US MKT HAO INSTRUMENT, SURGICAL, NON-POWERED 1 NA
40 00885074375458 SB7MAC30 CATHETER SB7MAC30 SB 7F 100CM MA30 DQY CATHETER, PERCUTANEOUS 2 SHERPA NX BALANCED
41 00885074372181 SB7EBU40D CATHETER SB7EBU40D SB 7F 90CM EB40 DQY CATHETER, PERCUTANEOUS 2 SHERPA NX BALANCED
42 00763000665982 BB11V67R3 CUSTOM PACK BB11V67R3 UMC DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
43 00763000552985 CB11J56R3 CUSTOM PACK CB11J56R3 PEDI MAG DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
44 00763000541118 6A32R2 CUSTOM PACK 6A32R2 1/4X1/4 DWF Catheter, cannula and tubing, vascular, cardiopulmonary bypass 2 NA
45 00763000400866 3320L LIT 3320L DYSTONIA EMANUALS EN MRU implanted subcortical electrical Stimulator (motor disorders) N/A
46 00763000502843 FMET-IM-SYS-S SYSTEM SERVICED FMET-IM-SYS-S DPW FLOWMETER, BLOOD, CARDIOVASCULAR 2 FlowMet™
47 00763000390891 LA6ERADRST CATHETER LA6ERADRST LA 6F 100CM ERDRS DQY Catheter, percutaneous 2 Launcher
48 00763000310332 37601 INS 37601 ACTIVA PC DBS EMANUAL EN OLM,MRU,MHY,NHL,MBX,PJS Deep brain stimulator for obsessive compulsive disorder (OCD),implanted subcorti Deep brain stimulator for obsessive compulsive disorder (OCD),implanted subcortical electrical Stimulator (motor disorders),STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR,Stimulator, electrical, implanted, for parkinsonian symptoms,STIMULATOR, THALAMIC, EPILEPSY, IMPLANTED,Stimulator, electrical, implanted, for essential tremor 3 Activa® PC
49 00763000306519 104FS FOOTSWITCH 104FS CRYOCONSOLE MDR LPB Cardiac ablation percutaneous catheter 3 N/A
50 00763000301330 HC150A HANDCRANK HC150A PLX 31L DWA Control, pump speed, cardiopulmonary bypass 2 Affinity™
Other products with the same Product Code "JPA"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00842768026812 10487098 ORKL19 Standard Human Plasma for the calibration of coagulation and fibrinolysis tests Standard Human Plasma SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
2 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
3 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
4 00842768014222 10446232 ORHO37 Supplementary Reagent for coagulation tests Calcium Chloride Solution SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
5 00842768012358 10446541 OVMN11 The cuvettes serve coagulation tests as a reaction vessel. Cuvettes for BFT // Analyzer SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
6 00842768012259 10446530 OVKG03 The cuvettes serve coagulation tests as a reaction vessel. BFT II Analyzer Dispo System SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
7 00842768006869 10445989 OPCC03 For calibration of the Berichrom Heparin assay for measurement of unfractionated heparin Berichrom® Heparin UF Calibrator SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH
8 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
9 00817869020311 SC-125, SC-126, H2O Hemotec Whole Blood Control Kit Large ANALYTICAL CONTROL SYSTEMS INC
10 00817869020274 SC-127 SC-127 Whole Blood Control Level III ANALYTICAL CONTROL SYSTEMS INC
11 00817869020267 SC-126 SC-126 Whole Blood Control Level II ANALYTICAL CONTROL SYSTEMS INC
12 00817869020250 SC-125 SC-125 Whole Blood Control Level I ANALYTICAL CONTROL SYSTEMS INC
13 00817869020007 CR-109 CR-109 .02M Calcium Chloride ANALYTICAL CONTROL SYSTEMS INC
14 00673978519173 550-90 CONTROL TEST 550-90 PROFICIENCY 5L NA MEDTRONIC, INC.
15 00613994615633 313-51 DEVICE 313-51 HEPTRAC ELEC QLT CNTRL CEM HEPtrac® MEDTRONIC, INC.
16 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.
17 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.
18 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.
19 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.
20 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.
21 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.
22 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.
23 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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