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 |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 00818354017571 | 2006 | 2006 | Large Occlusion Balloon Catheter | EndoCATH | ATRICURE, INC. |
2 | 00818075010080 | 27B | PL273-150-001 | Catheter | Plato | SCIENTIA VASCULAR LLC |
3 | 00818075010080 | 27B | PL273-150-001 | Catheter | Plato | SCIENTIA VASCULAR LLC |
4 | 00818053023002 | ECL2L6x20 | N/A | ECLIPSE 2L balloon catheters are catheters with dual lumen arranged in parallel ECLIPSE 2L balloon catheters are catheters with dual lumen arranged in parallel configuration. The guidewire lumen or the working lumen is DMSO compatible and can be used for infusion/delivery of diagnostic and therapeutic devices. The inflation lumen is used for the inflation and deflation of the balloon. The inflation and deflation of the balloon can be achieved independently of the presence of the guidewire. ECLIPSE 2L balloon catheter is equipped with a non-detachable low inflation pressure super compliant balloon welded to the distal end of the catheter. | ECLIPSE 2L | BALT USA LLC |
5 | 00818053022982 | ECL2L6x15 | N/A | ECLIPSE 2L balloon catheters are catheters with dual lumen arranged in parallel ECLIPSE 2L balloon catheters are catheters with dual lumen arranged in parallel configuration. The guidewire lumen or the working lumen is DMSO compatible and can be used for infusion/delivery of diagnostic and therapeutic devices. The inflation lumen is used for the inflation and deflation of the balloon. The inflation and deflation of the balloon can be achieved independently of the presence of the guidewire. ECLIPSE 2L balloon catheter is equipped with a non-detachable low inflation pressure super compliant balloon welded to the distal end of the catheter. | ECLIPSE 2L | BALT USA LLC |
6 | 00818053022968 | ECL2L6x12 | N/A | ECLIPSE 2L balloon catheters are catheters with dual lumen arranged in parallel ECLIPSE 2L balloon catheters are catheters with dual lumen arranged in parallel configuration. The guidewire lumen or the working lumen is DMSO compatible and can be used for infusion/delivery of diagnostic and therapeutic devices. The inflation lumen is used for the inflation and deflation of the balloon. The inflation and deflation of the balloon can be achieved independently of the presence of the guidewire. ECLIPSE 2L balloon catheter is equipped with a non-detachable low inflation pressure super compliant balloon welded to the distal end of the catheter. | ECLIPSE 2L | BALT USA LLC |
7 | 00818053022944 | ECL2L6x9 | N/A | ECLIPSE 2L balloon catheters are catheters with dual lumen arranged in parallel ECLIPSE 2L balloon catheters are catheters with dual lumen arranged in parallel configuration. The guidewire lumen or the working lumen is DMSO compatible and can be used for infusion/delivery of diagnostic and therapeutic devices. The inflation lumen is used for the inflation and deflation of the balloon. The inflation and deflation of the balloon can be achieved independently of the presence of the guidewire. ECLIPSE 2L balloon catheter is equipped with a non-detachable low inflation pressure super compliant balloon welded to the distal end of the catheter. | ECLIPSE 2L | BALT USA LLC |
8 | 00818053022937 | ECL2L6x7SN | N/A | ECLIPSE 2L balloon catheters are catheters with dual lumen arranged in parallel ECLIPSE 2L balloon catheters are catheters with dual lumen arranged in parallel configuration. The guidewire lumen or the working lumen is DMSO compatible and can be used for infusion/delivery of diagnostic and therapeutic devices. The inflation lumen is used for the inflation and deflation of the balloon. The inflation and deflation of the balloon can be achieved independently of the presence of the guidewire. ECLIPSE 2L balloon catheter is equipped with a non-detachable low inflation pressure super compliant balloon welded to the distal end of the catheter. | ECLIPSE 2L | BALT USA LLC |
9 | 00818053022920 | ECL2L6x7 | N/A | ECLIPSE 2L balloon catheters are catheters with dual lumen arranged in parallel ECLIPSE 2L balloon catheters are catheters with dual lumen arranged in parallel configuration. The guidewire lumen or the working lumen is DMSO compatible and can be used for infusion/delivery of diagnostic and therapeutic devices. The inflation lumen is used for the inflation and deflation of the balloon. The inflation and deflation of the balloon can be achieved independently of the presence of the guidewire. ECLIPSE 2L balloon catheter is equipped with a non-detachable low inflation pressure super compliant balloon welded to the distal end of the catheter. | ECLIPSE 2L | BALT USA LLC |
10 | 00818053022913 | BALLAST105 | N/A | The Ballast 088 Long Sheath is a sterile, single use, single lumen, variable sti The Ballast 088 Long Sheath is a sterile, single use, single lumen, variable stiffness guide catheter/long sheath that is designed for facilitating the introduction of appropriately sized interventional devices into target blood vessels in the peripheral, coronary, and neuro vasculature. | Ballast 088 Long Sheath | BALT USA LLC |
11 | 00818053022906 | BALLAST100 | N/A | The Ballast 088 Long Sheath is a sterile, single use, single lumen, variable sti The Ballast 088 Long Sheath is a sterile, single use, single lumen, variable stiffness guide catheter/long sheath that is designed for facilitating the introduction of appropriately sized interventional devices into target blood vessels in the peripheral, coronary, and neuro vasculature. | Ballast 088 Long Sheath | BALT USA LLC |
12 | 00818053022890 | BALLAST90 | N/A | The Ballast 088 Long Sheath is a sterile, single use, single lumen, variable sti The Ballast 088 Long Sheath is a sterile, single use, single lumen, variable stiffness guide catheter/long sheath that is designed for facilitating the introduction of appropriately sized interventional devices into target blood vessels in the peripheral, coronary, and neuro vasculature. | Ballast 088 Long Sheath | BALT USA LLC |
13 | 00818053022883 | BALLAST80 | N/A | The Ballast 088 Long Sheath is a sterile, single use, single lumen, variable sti The Ballast 088 Long Sheath is a sterile, single use, single lumen, variable stiffness guide catheter/long sheath that is designed for facilitating the introduction of appropriately sized interventional devices into target blood vessels in the peripheral, coronary, and neuro vasculature. | Ballast 088 Long Sheath | BALT USA LLC |
14 | 00818053022838 | MA1.5FOLIVEMP | Magic Infusion Catheter is intended to operate for regional infusion of contrast Magic Infusion Catheter is intended to operate for regional infusion of contrast materials into selected vessels in the neurovasculature. Magic Infusion Catheters are intended to facilitate access through distant, tortuous vasculature. Progressive suppleness ranging from a highly flexible tip to a semi-rigid proximal section allows the catheter to be advanced by the physician. It is not intended for use in the coronary vasculature. | Magic Infusion Catheter | BALT USA LLC | |
15 | 00818053022821 | MA1.2FOLIVE | Magic Infusion Catheter is intended to operate for regional infusion of contrast Magic Infusion Catheter is intended to operate for regional infusion of contrast materials into selected vessels in the neurovasculature. Magic Infusion Catheters are intended to facilitate access through distant, tortuous vasculature. Progressive suppleness ranging from a highly flexible tip to a semi-rigid proximal section allows the catheter to be advanced by the physician. It is not intended for use in the coronary vasculature. | Magic Infusion Catheter | BALT USA LLC | |
16 | 00818053022647 | MAGICSTD | Magic Infusion Catheter is intended to operate for regional infusion of contrast Magic Infusion Catheter is intended to operate for regional infusion of contrast materials into selected vessels in the neurovasculature. Magic Infusion Catheters are intended to facilitate access through distant, tortuous vasculature. Progressive suppleness ranging from a highly flexible tip to a semi-rigid proximal section allows the catheter to be advanced by the physician. It is not intended for use in the coronary vasculature. | Magic Infusion Catheter | BALT USA LLC | |
17 | 00818053022630 | MAGICMP | Magic Infusion Catheter is intended to operate for regional infusion of contrast Magic Infusion Catheter is intended to operate for regional infusion of contrast materials into selected vessels in the neurovasculature. Magic Infusion Catheters are intended to facilitate access through distant, tortuous vasculature. Progressive suppleness ranging from a highly flexible tip to a semi-rigid proximal section allows the catheter to be advanced by the physician. It is not intended for use in the coronary vasculature. | Magic Infusion Catheter | BALT USA LLC | |
18 | 00818053022623 | MA1.5FMP | Magic Infusion Catheter is intended to operate for regional infusion of contrast Magic Infusion Catheter is intended to operate for regional infusion of contrast materials into selected vessels in the neurovasculature. Magic Infusion Catheters are intended to facilitate access through distant, tortuous vasculature. Progressive suppleness ranging from a highly flexible tip to a semi-rigid proximal section allows the catheter to be advanced by the physician. It is not intended for use in the coronary vasculature. | Magic Infusion Catheter | BALT USA LLC | |
19 | 00818053022616 | MAGIC1.5F | Magic Infusion Catheter is intended to operate for regional infusion of contrast Magic Infusion Catheter is intended to operate for regional infusion of contrast materials into selected vessels in the neurovasculature. Magic Infusion Catheters are intended to facilitate access through distant, tortuous vasculature. Progressive suppleness ranging from a highly flexible tip to a semi-rigid proximal section allows the catheter to be advanced by the physician. It is not intended for use in the coronary vasculature. | Magic Infusion Catheter | BALT USA LLC | |
20 | 00818053022609 | MAGIC1.2FM180 | Magic Infusion Catheter is intended to operate for regional infusion of contrast Magic Infusion Catheter is intended to operate for regional infusion of contrast materials into selected vessels in the neurovasculature. Magic Infusion Catheters are intended to facilitate access through distant, tortuous vasculature. Progressive suppleness ranging from a highly flexible tip to a semi-rigid proximal section allows the catheter to be advanced by the physician. It is not intended for use in the coronary vasculature. | Magic Infusion Catheter | BALT USA LLC | |
21 | 00818053022593 | MAGIC1.2FM | Magic Infusion Catheter is intended to operate for regional infusion of contrast Magic Infusion Catheter is intended to operate for regional infusion of contrast materials into selected vessels in the neurovasculature. Magic Infusion Catheters are intended to facilitate access through distant, tortuous vasculature. Progressive suppleness ranging from a highly flexible tip to a semi-rigid proximal section allows the catheter to be advanced by the physician. It is not intended for use in the coronary vasculature. | Magic Infusion Catheter | BALT USA LLC | |
22 | 00818053022586 | MAGIC1.2F | Magic Infusion Catheter is intended to operate for regional infusion of contrast Magic Infusion Catheter is intended to operate for regional infusion of contrast materials into selected vessels in the neurovasculature. Magic Infusion Catheters are intended to facilitate access through distant, tortuous vasculature. Progressive suppleness ranging from a highly flexible tip to a semi-rigid proximal section allows the catheter to be advanced by the physician. It is not intended for use in the coronary vasculature. | Magic Infusion Catheter | BALT USA LLC | |
23 | 00816900020334 | GEN-10815-125 | GEN-10815-125 | Intermediate Catheter, Hemostasis Valve, & Introducer | SYPHONTRAK | INNEUROCO, INC. |
24 | 00816900020327 | GEN-10815-115 | GEN-10815-115 | Intermediate Catheter, Hemostasis Valve, & Introducer | SYPHONTRAK | INNEUROCO, INC. |
25 | 00816900020310 | GEN-10815-105 | GEN-10815-105 | Intermediate Catheter, Hemostasis Valve, & Introducer | SYPHONTRAK | INNEUROCO, INC. |
26 | 00816900020273 | GEN-10820-135 | GEN-10820-135 | Catheter, Hemostasis Valve, & Introducer | SYPHONTRAK SDA | INNEUROCO, INC. |
27 | 00816900020266 | GEN-10820-125 | GEN-10820-125 | Catheter, Hemostasis Valve, & Introducer | SYPHONTRAK SDA | INNEUROCO, INC. |
28 | 00816900020259 | GEN-10820-115 | GEN-10820-115 | Catheter, Hemostasis Valve, & Introducer | SYPHONTRAK SDA | INNEUROCO, INC. |
29 | 00816900020099 | GEN-10820-135 | GEN-10820-135 | Catheter, Hemostasis Valve, & Introducer | Super Distal Access (SDA) | INNEUROCO, INC. |
30 | 00816900020082 | GEN-10820-125 | GEN-10820-125 | Catheter, Hemostasis Valve, & Introducer | Super Distal Access (SDA) | INNEUROCO, INC. |
31 | 00816900020075 | GEN-10820-115 | GEN-10820-115 | Catheter, Hemostasis Valve, & Introducer | Super Distal Access (SDA) | INNEUROCO, INC. |
32 | 00816900020037 | GEN-10815-105 | GEN-10815-105 | Intermediate Catheter, Hemostasis Valve, & Introducer | Intermediate Catheter | INNEUROCO, INC. |
33 | 00816900020020 | GEN-10815-125 | GEN-10815-125 | Intermediate Catheter, Hemostasis Valve, & Introducer | Intermediate Catheter | INNEUROCO, INC. |
34 | 00816900020013 | GEN-10815-115 | GEN-10815-115 | Intermediate Catheter, Hemostasis Valve, & Introducer | Intermediate Catheter | INNEUROCO, INC. |
35 | 00816840020807 | PMC-005 | Poseidon | HERAEUS MEDICAL COMPONENTS LLC | ||
36 | 00816840020807 | PMC-005 | Poseidon | HERAEUS MEDICAL COMPONENTS LLC | ||
37 | 00816840020791 | PMC-004 | Poseidon | HERAEUS MEDICAL COMPONENTS LLC | ||
38 | 00816840020791 | PMC-004 | Poseidon | HERAEUS MEDICAL COMPONENTS LLC | ||
39 | 00816777025920 | DA5115ST-E | DA5115ST | Stroke Access | Sofia 5F-115cm STR | MICROVENTION INC. |
40 | 00816777025913 | DA5125ST-E | DA5125ST | Stroke Access | Sofia 5F-125cm STR | MICROVENTION INC. |
41 | 00816777025838 | MCWED21160 | MCWED21160 | Microcatheter | Wedge | MICROVENTION INC. |
42 | 00815948024083 | PNS6F105BER-R | Neuron 6F Select, 105cm, Berenstein | Neuron | PENUMBRA, INC. | |
43 | 00815948024076 | PNS6F105H1-R | Neuron 6F Select, 105cm, H1 | Neuron | PENUMBRA, INC. | |
44 | 00815948024069 | PNS6F125SIMV-R | Neuron 6F Select, 120cm, Sim-V | Neuron | PENUMBRA, INC. | |
45 | 00815948024052 | PNS6F125BER-R | Neuron 6F Select, 125cm, Berenstein | Neuron | PENUMBRA, INC. | |
46 | 00815948024045 | PNS6F125H1-R | Neuron 6F Select, 125cm, H1 | Neuron | PENUMBRA, INC. | |
47 | 00815948024038 | PNS6F125SIM-R | Neuron 6F Select, 125cm, Simmons | Neuron | PENUMBRA, INC. | |
48 | 00815948023086 | BMX96100MSIMV125-A | BMX96 100cm, MP Tip, 6F SIMV 125cm Select | Benchmark MAX System | PENUMBRA, INC. | |
49 | 00815948023079 | BMX96100SIMV125-A | BMX96 100cm, STR Tip, 6F SIMV 125cm Select | Benchmark MAX System | PENUMBRA, INC. | |
50 | 00815948023062 | BMX96100MBER125-A | BMX96 100cm, MP Tip, 6F BER 125cm Select | Benchmark MAX System | PENUMBRA, INC. |