| 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 | 04544050120746 | 1610590 | The CELLO Balloon Guide Catheter is indicated for use in facilitating the insert The CELLO Balloon Guide Catheter is indicated for use in facilitating the insertion and guidance of intravascular catheters into a selected blood vessel in the peripheral and neuro vasculature systems. The balloon provides temporary vascular occlusion during these and other angiographic procedures. | CELLO™, Balloon Guide Catheter | FUJI SYSTEMS CORPORATION | |
| 2 | 04544050120739 | 1610580 | The CELLO Balloon Guide Catheter is indicated for use in facilitating the insert The CELLO Balloon Guide Catheter is indicated for use in facilitating the insertion and guidance of intravascular catheters into a selected blood vessel in the peripheral and neuro vasculature systems. The balloon provides temporary vascular occlusion during these and other angiographic procedures. | CELLO™, Balloon Guide Catheter | FUJI SYSTEMS CORPORATION | |
| 3 | 04544050120722 | 1610570 | The CELLO Balloon Guide Catheter is indicated for use in facilitating the insert The CELLO Balloon Guide Catheter is indicated for use in facilitating the insertion and guidance of intravascular catheters into a selected blood vessel in the peripheral and neuro vasculature systems. The balloon provides temporary vascular occlusion during these and other angiographic procedures. | CELLO™, Balloon Guide Catheter | FUJI SYSTEMS CORPORATION | |
| 4 | 04544050120715 | 1610560 | The CELLO Balloon Guide Catheter is indicated for use in facilitating the insert The CELLO Balloon Guide Catheter is indicated for use in facilitating the insertion and guidance of intravascular catheters into a selected blood vessel in the peripheral and neuro vasculature systems. The balloon provides temporary vascular occlusion during these and other angiographic procedures. | CELLO™, Balloon Guide Catheter | FUJI SYSTEMS CORPORATION | |
| 5 | 04544050093491 | 9F | 1610590 | The CELLO Balloon Guide Catheter is indicated for use in facilitating the insert The CELLO Balloon Guide Catheter is indicated for use in facilitating the insertion and guidance of intravascular catheters into a selected blood vessel in the peripheral and neuro vasculature systems. The balloon provides temporary vascular occlusion during these and other angiographic procedures. | CELLO™, Balloon Guide Catheter | FUJI SYSTEMS CORPORATION |
| 6 | 04544050093484 | 8F | 1610580 | The CELLO Balloon Guide Catheter is indicated for use in facilitating the insert The CELLO Balloon Guide Catheter is indicated for use in facilitating the insertion and guidance of intravascular catheters into a selected blood vessel in the peripheral and neuro vasculature systems. The balloon provides temporary vascular occlusion during these and other angiographic procedures. | CELLO™, Balloon Guide Catheter | FUJI SYSTEMS CORPORATION |
| 7 | 04544050093460 | 7F | 1610570 | The CELLO Balloon Guide Catheter is indicated for use in facilitating the insert The CELLO Balloon Guide Catheter is indicated for use in facilitating the insertion and guidance of intravascular catheters into a selected blood vessel in the peripheral and neuro vasculature systems. The balloon provides temporary vascular occlusion during these and other angiographic procedures. | CELLO™, Balloon Guide Catheter | FUJI SYSTEMS CORPORATION |
| 8 | 04544050093446 | 6F | 1610560 | The CELLO Balloon Guide Catheter is indicated for use in facilitating the insert The CELLO Balloon Guide Catheter is indicated for use in facilitating the insertion and guidance of intravascular catheters into a selected blood vessel in the peripheral and neuro vasculature systems. The balloon provides temporary vascular occlusion during these and other angiographic procedures. | CELLO™, Balloon Guide Catheter | FUJI SYSTEMS CORPORATION |
| 9 | 04540778154193 | BD-L70200ER | BD-L70200ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 10 | 04540778154179 | BD-L60200ER | BD-L60200ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 11 | 04540778154155 | BD-L50200ER | BD-L50200ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 12 | 04540778154131 | BD-L40200ER | BD-L40200ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 13 | 04540778154117 | BD-L30200ER | BD-L30200ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 14 | 04540778154094 | BD-L70150ER | BD-L70150ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 15 | 04540778154070 | BD-L60150ER | BD-L60150ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 16 | 04540778154056 | BD-L50150ER | BD-L50150ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 17 | 04540778154032 | BD-L40150ER | BD-L40150ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 18 | 04540778154018 | BD-L30150ER | BD-L30150ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 19 | 04540778153998 | BD-L70120ER | BD-L70120ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 20 | 04540778153974 | BD-L60120ER | BD-L60120ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 21 | 04540778153950 | BD-L50120ER | BD-L50120ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 22 | 04540778153936 | BD-L40120ER | BD-L40120ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 23 | 04540778153912 | BD-L30120ER | BD-L30120ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 24 | 04540778153899 | BD-L70100ER | BD-L70100ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 25 | 04540778153875 | BD-L60100ER | BD-L60100ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 26 | 04540778153851 | BD-L50100ER | BD-L50100ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 27 | 04540778153837 | BD-L40100ER | BD-L40100ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 28 | 04540778153813 | BD-L30100ER | BD-L30100ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 29 | 04540778153790 | BD-LX0080ER | BD-LX0080ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 30 | 04540778153776 | BD-L90080ER | BD-L90080ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 31 | 04540778153752 | BD-L80080ER | BD-L80080ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 32 | 04540778153738 | BD-L70080ER | BD-L70080ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 33 | 04540778153714 | BD-L60080ER | BD-L60080ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 34 | 04540778153691 | BD-L50080ER | BD-L50080ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 35 | 04540778153677 | BD-L40080ER | BD-L40080ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 36 | 04540778153653 | BD-L30080ER | BD-L30080ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 37 | 04540778153639 | BD-LX0060ER | BD-LX0060ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 38 | 04540778153615 | BD-L90060ER | BD-L90060ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 39 | 04540778153592 | BD-L80060ER | BD-L80060ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 40 | 04540778153578 | BD-L70060ER | BD-L70060ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 41 | 04540778153554 | BD-L60060ER | BD-L60060ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 42 | 04540778153530 | BD-L50060ER | BD-L50060ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 43 | 04540778153516 | BD-L40060ER | BD-L40060ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 44 | 04540778153493 | BD-L30060ER | BD-L30060ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 45 | 04540778153479 | BD-LX2040ER | BD-LX2040ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 46 | 04540778153455 | BD-LX0040ER | BD-LX0040ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 47 | 04540778153431 | BD-L90040ER | BD-L90040ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 48 | 04540778153417 | BD-L80040ER | BD-L80040ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 49 | 04540778153394 | BD-L70040ER | BD-L70040ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |
| 50 | 04540778153370 | BD-L60040ER | BD-L60040ER | METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation METACROSS RX is a Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter for peripheral indications. METACROSS RX is a rapid exchange (RX) type and the maximum diameter of the compatible guidewire is 0.035 inches (0.89 mm). | METACROSS RX | KANEKA CORPORATION |