Other products from "MICRO THERAPEUTICS, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00763000284077 PED2-325-16 STENT PED2-325-16 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
2 00763000284046 PED2-325-10 STENT PED2-325-10 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
3 00763000284022 PED2-300-30 STENT PED2-300-30 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
4 00763000283964 PED2-300-12 STENT PED2-300-12 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
5 00763000283957 PED2-300-10 STENT PED2-300-10 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
6 00763000283940 PED2-275-20 STENT PED2-275-20 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
7 00847536034747 SFR3-4-20-05 STENT SFR3-4-20-05 V06 ENHANCED POL,NRY Neurovascular Mechanical Thrombectomy Device for Acute Ischemic Stroke Treatment Neurovascular Mechanical Thrombectomy Device for Acute Ischemic Stroke Treatment,CATHETER, THROMBUS RETRIEVER 2 Solitaire™ Platinum
8 00847536034730 SFR4-6-40-10 STENT SFR4-6-40-10 V01 US NRY,POL CATHETER, THROMBUS RETRIEVER,Neurovascular Mechanical Thrombectomy Device for Ac CATHETER, THROMBUS RETRIEVER,Neurovascular Mechanical Thrombectomy Device for Acute Ischemic Stroke Treatment 2 Solitaire™ X
9 00847536034716 SFR4-6-20-10 STENT SFR4-6-20-10 V01 US POL,NRY Neurovascular Mechanical Thrombectomy Device for Acute Ischemic Stroke Treatment Neurovascular Mechanical Thrombectomy Device for Acute Ischemic Stroke Treatment,CATHETER, THROMBUS RETRIEVER 2 Solitaire™ X
10 00847536006836 41047-01 INF CATH 41047-01 CRAGG-MCNAMARA V03 FOZ Catheter,intravascular,therapeutic,short-term less than 30 days 2 Cragg McNamaraTM
11 00847536006812 41046-01 INF CATH 41046-01 CRAGG-MCNAMARA V03 FOZ Catheter,intravascular,therapeutic,short-term less than 30 days 2 Cragg McNamaraTM
12 00847536006591 41035-01 INF CATH 41035-01 CRAGG-MCNAMARA V03 FOZ Catheter,intravascular,therapeutic,short-term less than 30 days 2 Cragg McNamaraTM
13 00847536006553 41033-01 INF CATH 41033-01 CRAGG-MCNAMARA V03 FOZ Catheter,intravascular,therapeutic,short-term less than 30 days 2 Cragg McNamaraTM
14 00847536006188 105-7100-080 105-7100-080 ONYX 34 KIT AVM US MFE Agent, injectable, embolic 3 ONYX 34
15 00847536007048 41057-01 INF CATH 41057-01 CRAGG-MCNAMARA V04 FOZ Catheter,intravascular,therapeutic,short-term less than 30 days 2 Cragg McNamaraTM
16 00763000284756 PED2-500-35 STENT PED2-500-35 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
17 00763000284749 PED2-500-30 STENT PED2-500-30 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
18 00763000284732 PED2-500-25 STENT PED2-500-25 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
19 00763000284664 PED2-475-35 STENT PED2-475-35 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
20 00763000284657 PED2-475-30 STENT PED2-475-30 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
21 00763000284640 PED2-475-25 STENT PED2-475-25 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
22 00763000284633 PED2-475-20 STENT PED2-475-20 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
23 00763000284626 PED2-475-18 STENT PED2-475-18 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
24 00763000284619 PED2-475-16 STENT PED2-475-16 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
25 00763000284602 PED2-475-14 STENT PED2-475-14 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
26 00763000284596 PED2-475-12 STENT PED2-475-12 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
27 00763000284589 PED2-475-10 STENT PED2-475-10 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
28 00763000284572 PED2-450-35 STENT PED2-450-35 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
29 00763000284565 PED2-450-30 STENT PED2-450-30 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
30 00763000284558 PED2-450-25 STENT PED2-450-25 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
31 00763000284541 PED2-450-20 STENT PED2-450-20 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
32 00763000284534 PED2-450-18 STENT PED2-450-18 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
33 00763000284527 PED2-450-16 STENT PED2-450-16 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
34 00763000284510 PED2-450-14 STENT PED2-450-14 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
35 00763000284503 PED2-450-12 STENT PED2-450-12 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
36 00763000284497 PED2-450-10 STENT PED2-450-10 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
37 00763000284725 PED2-500-20 STENT PED2-500-20 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
38 00763000284718 PED2-500-18 STENT PED2-500-18 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
39 00763000284701 PED2-500-16 STENT PED2-500-16 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
40 00763000284695 PED2-500-14 STENT PED2-500-14 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
41 00763000284688 PED2-500-12 STENT PED2-500-12 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
42 00763000284671 PED2-500-10 STENT PED2-500-10 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
43 00763000284480 PED2-425-35 STENT PED2-425-35 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
44 00763000284473 PED2-425-30 STENT PED2-425-30 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
45 00763000284466 PED2-425-25 STENT PED2-425-25 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
46 00763000284459 PED2-425-20 STENT PED2-425-20 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
47 00763000284442 PED2-425-18 STENT PED2-425-18 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
48 00763000284435 PED2-425-16 STENT PED2-425-16 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
49 00763000284428 PED2-425-14 STENT PED2-425-14 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
50 00763000284411 PED2-425-12 STENT PED2-425-12 V06 E-IFU OUT Intracranial aneurysm flow diverter 3 PipelineTM Flex Embolization Device with Shield TechnologyTM
Other products with the same Product Code "DQX"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 M58800101005611 1 001-010056-1 "The Vdrive® system is intended to stabilize, navigate and remotely control: • C "The Vdrive® system is intended to stabilize, navigate and remotely control: • Compatible Intracardiac Echocardiography (ICE) catheters to facilitate visualization of cardiac structure during theperformance of cardiac procedure when used in conjunction with the V-Sono™ disposable sets in the Vdrive® system, • Compatible loop (circular) mapping catheters to facilitate movement of the catheter during the performance ofelectrophysiological procedures when used in conjunction with the V-Loop™ disposable sets in the Vdrive® system, and • Compatible fixed curve transseptal sheaths and catheters to facilitate movement of the sheath and catheter when usedin conjunction with the V-CAS™ disposable sets in the Vdrive® system and with the Niobe® Magnetic NavigationSystem (MNS). " Vdrive Drape STEREOTAXIS, INC.
2 M58800100411590 II 001-004115-9 The Stereotaxis Cardiodrive is intended for automatically advancing and retracti The Stereotaxis Cardiodrive is intended for automatically advancing and retracting only compatible magnetic electrophysiology (EP) mapping and ablation catheters inside the patient's heart when used in conjunction with a Stereotaxis Magnetic Navigation System (MNS). It is not intended to advance the EP mapping and ablation catheters through the coronary vasculature nor the coronary sinus. Cardiodrive System STEREOTAXIS, INC.
3 M588001004115120 II 001-004115-12 The Stereotaxis Cardiodrive is intended for automatically advancing and retracti The Stereotaxis Cardiodrive is intended for automatically advancing and retracting only compatible magnetic electrophysiology (EP) mapping and ablation catheters inside the patient's heart when used in conjunction with a Stereotaxis Magnetic Navigation System (MNS). It is not intended to advance the EP mapping and ablation catheters through the coronary vasculature nor the coronary sinus. Cardiodrive System STEREOTAXIS, INC.
4 M588001004115110 II 001-004115-11 The Stereotaxis Cardiodrive is intended for automatically advancing and retracti The Stereotaxis Cardiodrive is intended for automatically advancing and retracting only compatible magnetic electrophysiology (EP) mapping and ablation catheters inside the patient's heart when used in conjunction with a Stereotaxis Magnetic Navigation System (MNS). It is not intended to advance the EP mapping and ablation catheters through the coronary vasculature nor the coronary sinus. Cardiodrive System STEREOTAXIS, INC.
5 M58800100246910 1 001-002469-1 Vdrive with V-Sono is indicated for remotely controlling the advancement, retrac Vdrive with V-Sono is indicated for remotely controlling the advancement, retraction, rotation and anterior-posterior deflection of compatible ultrasound catheters inserted into the right atrium V-Sono Intracardiac Echo Manipulator STEREOTAXIS, INC.
6 M58800100245210 1 001-002452-1 The Vdrive with V-Loop disposable is indicated to remotely control the advanceme The Vdrive with V-Loop disposable is indicated to remotely control the advancement, retraction, rotation, tip deflection and loop size of compatibile loop catheters inserted across the septum into the left atrium using conventional procedures V-Loop Variable Loop Catheter Manipulator STEREOTAXIS, INC.
7 M58800100242210 1 001-002422-1 The Vdrive with V-CAS Disposable is indicated for remotely controlling the advan The Vdrive with V-CAS Disposable is indicated for remotely controlling the advancement, retraction, and rotation of compatible magnetic electrophysiology (EP) mapping and ablation catheters inside the patient's heart when used in conjunction with a Stereotaxis Magnetic Navigation System V-CAS Catheter Advancement System STEREOTAXIS, INC.
8 M58800100230720 Duo 001-002307-2 "The Vdrive® system is intended to stabilize, navigate and remotely control: • C "The Vdrive® system is intended to stabilize, navigate and remotely control: • Compatible Intracardiac Echocardiography (ICE) catheters to facilitate visualization of cardiac structure during theperformance of cardiac procedure when used in conjunction with the V-Sono™ disposable sets in the Vdrive® system, • Compatible loop (circular) mapping catheters to facilitate movement of the catheter during the performance ofelectrophysiological procedures when used in conjunction with the V-Loop™ disposable sets in the Vdrive® system, and • Compatible fixed curve transseptal sheaths and catheters to facilitate movement of the sheath and catheter when usedin conjunction with the V-CAS™ disposable sets in the Vdrive® system and with the Niobe® Magnetic NavigationSystem (MNS). " Vdrive System STEREOTAXIS, INC.
9 M58800100230710 Single Arm 001-002307-1 "The Vdrive® system is intended to stabilize, navigate and remotely control: • C "The Vdrive® system is intended to stabilize, navigate and remotely control: • Compatible Intracardiac Echocardiography (ICE) catheters to facilitate visualization of cardiac structure during theperformance of cardiac procedure when used in conjunction with the V-Sono™ disposable sets in the Vdrive® system, • Compatible loop (circular) mapping catheters to facilitate movement of the catheter during the performance ofelectrophysiological procedures when used in conjunction with the V-Loop™ disposable sets in the Vdrive® system, and • Compatible fixed curve transseptal sheaths and catheters to facilitate movement of the sheath and catheter when usedin conjunction with the V-CAS™ disposable sets in the Vdrive® system and with the Niobe® Magnetic NavigationSystem (MNS). " Vdrive System STEREOTAXIS, INC.
10 M5880010017712 1 001-001771-2 The Stereotaxis Cardiodrive is intended for automatically advancing and retracti The Stereotaxis Cardiodrive is intended for automatically advancing and retracting only compatible magnetic electrophysiology (EP) mapping and ablation catheters inside the patient's heart when used in conjunction with a Stereotaxis Magnetic Navigation System (MNS). It is not intended to advance the EP mapping and ablation catheters through the coronary vasculature nor the coronary sinus. Cardiodrive Hemostasis Adapter - SJ STEREOTAXIS, INC.
11 M5880010017711 1 001-001771-1 The Stereotaxis Cardiodrive is intended for automatically advancing and retracti The Stereotaxis Cardiodrive is intended for automatically advancing and retracting only compatible magnetic electrophysiology (EP) mapping and ablation catheters inside the patient's heart when used in conjunction with a Stereotaxis Magnetic Navigation System (MNS). It is not intended to advance the EP mapping and ablation catheters through the coronary vasculature nor the coronary sinus. QuikCAS Hemostasis Adapter STEREOTAXIS, INC.
12 M58800100175110 1 001-001751-1 The Stereotaxis Cardiodrive is intended for automatically advancing and retracti The Stereotaxis Cardiodrive is intended for automatically advancing and retracting only compatible magnetic electrophysiology (EP) mapping and ablation catheters inside the patient's heart when used in conjunction with a Stereotaxis Magnetic Navigation System (MNS). It is not intended to advance the EP mapping and ablation catheters through the coronary vasculature nor the coronary sinus. QuikCAS Cardiodrive Sterile Components STEREOTAXIS, INC.
13 M58800100111411 IV-1 0010011141 Hemostasis Adapter IV Spares, Box, Device Count(5) Hemostasis Adapter STEREOTAXIS, INC.
14 10195327188955 DYNJGWIRE20L DYNJGWIRE20L GUIDEWIRE 3MMJ 0.035X260CM LT Medline Industries, Inc. MEDLINE INDUSTRIES, INC.
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