| 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 | 00863092000118 | ER7232A | ER7232A | ER-REBOA Catheter | PRYTIME MEDICAL DEVICES, INC. | |
| 2 | 00862468000318 | FG32101 | Peregrine System Infusion Catheter, US | Peregrine System Infusion Catheter | ABLATIVE SOLUTIONS, INC. | |
| 3 | 00860554000396 | CM-3600 | The Houdini Catheter is a single use, dual-lumen intravascular catheter intended The Houdini Catheter is a single use, dual-lumen intravascular catheter intended for percutaneous use.The Houdini Catheter is intended to be used in conjunction with a steerable guidewire to access discrete regions of the peripheral vasculature and for guidewire exchange. | Cruzar Medsystems Inc. | CRUZAR MEDSYSTEMS INC | |
| 4 | 00860554000365 | CM-3500 | The Houdini Catheter is a single use, dual-lumen intravascular catheter intended The Houdini Catheter is a single use, dual-lumen intravascular catheter intended for percutaneous use.The Houdini Catheter is intended to be used in conjunction with a steerable guidewire to access discrete regions of the peripheral vasculature and for guidewire exchange. | Cruzar Medsystems Inc. | CRUZAR MEDSYSTEMS INC | |
| 5 | 00860554000358 | CM-3800 | The Houdini Catheter is a single use, dual-lumen intravascular catheter intended The Houdini Catheter is a single use, dual-lumen intravascular catheter intended for percutaneous use.The Houdini Catheter is intended to be used in conjunction with a steerable guidewire to access discrete regions of the peripheral vasculature and for guidewire exchange. | Cruzar Medsystems Inc. | CRUZAR MEDSYSTEMS INC | |
| 6 | 00860554000334 | CM-3400 | The Houdini Catheter is a single use, dual-lumen intravascular catheter intended The Houdini Catheter is a single use, dual-lumen intravascular catheter intended for percutaneous use.The Houdini Catheter is intended to be used in conjunction with a steerable guidewire to access discrete regions of the peripheral vasculature and for guidewire exchange. | Cruzar Medsystems Inc. | CRUZAR MEDSYSTEMS INC | |
| 7 | 00860554000327 | CM-3700 | The Houdini Catheter is a single use, dual-lumen intravascular catheter intended The Houdini Catheter is a single use, dual-lumen intravascular catheter intended for percutaneous use.The Houdini Catheter is intended to be used in conjunction with a steerable guidewire to access discrete regions of the peripheral vasculature and for guidewire exchange. | Cruzar Medsystems Inc. | CRUZAR MEDSYSTEMS INC | |
| 8 | 00860003254615 | 100240-D | 100240-D | BOSS Balloon Guide Catheter, DEMO UNIT, Not for Human Use | Marblehead Medical | MARBLEHEAD MEDICAL LLC |
| 9 | 00860003254608 | 100240 | 100240 | BOSS Balloon Guide Catheter | Marblehead Medical | MARBLEHEAD MEDICAL LLC |
| 10 | 00859821006698 | 3Fr x 5cm | 96001 | The ARTERIAL WAND Safety Introducer with Arterial Catheter made of ChronoFlex C The ARTERIAL WAND Safety Introducer with Arterial Catheter made of ChronoFlex C with BioGUARD Technology | ARTERIAL WAND | ACCESS SCIENTIFIC, LLC |
| 11 | 00858593006509 | 700-10302 | 700-10302 | The Connector Interface Cable (CIC) is the cable assembly that connects the Infu The Connector Interface Cable (CIC) is the cable assembly that connects the Infusion Catheter and Ultrasonic Core to the Control Unit. | EkoSonic® | EKOS CORPORATION |
| 12 | 00858593006493 | 600-30000 | 600-30000 | The EkoSonic® Control Unit provides power to the Ultrasonic Core and monitors pa The EkoSonic® Control Unit provides power to the Ultrasonic Core and monitors parameters during operation via the CIC. The Control Unit also provides the user interface for operator control. The EkoSonic® Control Unit is intended exclusively for use with the EkoSonic® Device. | EkoSonic® | EKOS CORPORATION |
| 13 | 00858593006479 | EKOS Connector Interface Cable | 700-10410 | The Connector Interface Cable (CIC) is the cable assembly that connects the Infu The Connector Interface Cable (CIC) is the cable assembly that connects the Infusion Catheter and Ultrasonic Core to the Control Unit. | EKOS™ | BOSTON SCIENTIFIC CORPORATION |
| 14 | 00858593006462 | EKOS Control Unit 4.0 | 600-40500 | The EKOS™ Control Unit provides power to the Ultrasonic Core and monitors parame The EKOS™ Control Unit provides power to the Ultrasonic Core and monitors parameters during operation via the CIC. The Control Unit also provides the user interface for operator control. | EKOS™ | BOSTON SCIENTIFIC CORPORATION |
| 15 | 00858593006318 | 6795-007 | 500-56150 | The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic Core. The device delivers physician-specified fluids and ultrasound to the intravascular treatment site. It comes in different working lengths and treatment zones. | EkoSonic® | BOSTON SCIENTIFIC CORPORATION |
| 16 | 00858593006301 | 6795-006 | 500-56140 | The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic Core. The device delivers physician-specified fluids and ultrasound to the intravascular treatment site. It comes in different working lengths and treatment zones. | EkoSonic® | BOSTON SCIENTIFIC CORPORATION |
| 17 | 00858593006295 | 6795-005 | 500-56130 | The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic Core. The device delivers physician-specified fluids and ultrasound to the intravascular treatment site. It comes in different working lengths and treatment zones. | EkoSonic® | BOSTON SCIENTIFIC CORPORATION |
| 18 | 00858593006264 | 6795-002 | 500-56112 | The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic Core. The device delivers physician-specified fluids and ultrasound to the intravascular treatment site. It comes in different working lengths and treatment zones. | EkoSonic® | BOSTON SCIENTIFIC CORPORATION |
| 19 | 00858593006189 | 6779-007 | 500-55150 | The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic Core. The device delivers physician-specified fluids and ultrasound to the intravascular treatment site. It comes in different working lengths and treatment zones. | EkoSonic® | BOSTON SCIENTIFIC CORPORATION |
| 20 | 00858593006172 | 6779-006 | 500-55140 | The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic Core. The device delivers physician-specified fluids and ultrasound to the intravascular treatment site. It comes in different working lengths and treatment zones. | EkoSonic® | BOSTON SCIENTIFIC CORPORATION |
| 21 | 00858593006165 | 6779-005 | 500-55130 | The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic Core. The device delivers physician-specified fluids and ultrasound to the intravascular treatment site. It comes in different working lengths and treatment zones. | EkoSonic® | BOSTON SCIENTIFIC CORPORATION |
| 22 | 00858593006158 | 6779-004 | 500-55124 | The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic Core. The device delivers physician-specified fluids and ultrasound to the intravascular treatment site. It comes in different working lengths and treatment zones. | EkoSonic® | BOSTON SCIENTIFIC CORPORATION |
| 23 | 00858593006141 | 6779-003 | 500-55118 | The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic Core. The device delivers physician-specified fluids and ultrasound to the intravascular treatment site. It comes in different working lengths and treatment zones. | EkoSonic® | BOSTON SCIENTIFIC CORPORATION |
| 24 | 00858593006134 | 6779-002 | 500-55112 | The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic Core. The device delivers physician-specified fluids and ultrasound to the intravascular treatment site. It comes in different working lengths and treatment zones. | EkoSonic® | BOSTON SCIENTIFIC CORPORATION |
| 25 | 00858593006028 | 6779-001 | 500-55106 | The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and The EkoSonic® Endovascular Device consists of a single use Infusion Catheter and an Ultrasonic Core. The device delivers physician-specified fluids and ultrasound to the intravascular treatment site. It comes in different working lengths and treatment zones. | EkoSonic® | BOSTON SCIENTIFIC CORPORATION |
| 26 | 00858480007206 | RCX-2018 | MicroCross 18 Catheter, 135 cm, CE | ROXWOOD MEDICAL, INC. | ||
| 27 | 00858480007190 | RC-2018 | MicroCross 18 Catheter, 135 cm | ROXWOOD MEDICAL, INC. | ||
| 28 | 00858480007183 | RCX-1018 | MicroCross 18 Catheter , 90cm, CE | ROXWOOD MEDICAL, INC. | ||
| 29 | 00858480007176 | RC-1018 | MicroCross 18 Catheter, 90 cm | ROXWOOD MEDICAL, INC. | ||
| 30 | 00858480007169 | RCX-3014 | MicroCross 14 ES Catheter, 135cm, CE | ROXWOOD MEDICAL, INC. | ||
| 31 | 00858480007152 | RCX-2014 | MicroCross 14 Catheter, 135cm, CE | ROXWOOD MEDICAL, INC. | ||
| 32 | 00858480007145 | RC-3014 | MicroCross 14 ES Catheter, 135cm | ROXWOOD MEDICAL, INC. | ||
| 33 | 00858480007138 | RC-2014 | MicroCross 14 Catheter, 135cm | ROXWOOD MEDICAL, INC. | ||
| 34 | 00858480007121 | RCX-0018 | Micro18 MicroCross Catheter, CE | ROXWOOD MEDICAL, INC. | ||
| 35 | 00858480007114 | RCX-1014 | Micro14es MicroCross Catheter, CE | ROXWOOD MEDICAL, INC. | ||
| 36 | 00858480007107 | RCX-0014 | Micro14 MicroCross Catheter,CE | ROXWOOD MEDICAL, INC. | ||
| 37 | 00858480007091 | UCX-0100 | CenterCross Ultra Catheter, CE | ROXWOOD MEDICAL, INC. | ||
| 38 | 00858480007084 | MCX-0100 | MultiCross Catheter, CE | ROXWOOD MEDICAL, INC. | ||
| 39 | 00858480007077 | CCX-0100 | CenterCross Catheter,CE | ROXWOOD MEDICAL, INC. | ||
| 40 | 00858480007060 | LV-0100 | CenterCross Ultra LV Catheter | ROXWOOD MEDICAL, INC. | ||
| 41 | 00858480007053 | UC-0100 | CenterCross Ultra Catheter | ROXWOOD MEDICAL, INC. | ||
| 42 | 00858480007046 | MC-0100 | MultiCross Catheter | ROXWOOD MEDICAL, INC. | ||
| 43 | 00858480007039 | RC-1014 | Micro14es MicroCross Catheter | ROXWOOD MEDICAL, INC. | ||
| 44 | 00858480007022 | RC-0018 | Micro18 MicroCross Catheter | ROXWOOD MEDICAL, INC. | ||
| 45 | 00858480007015 | RC-0014 | Micro14 MicroCross Catheter | ROXWOOD MEDICAL, INC. | ||
| 46 | 00858480007008 | CC-0100 | CenterCross Catheter | ROXWOOD MEDICAL, INC. | ||
| 47 | 00857834006933 | OMC003 | Odyssey Micro Catheter | HERAEUS MEDICAL COMPONENTS LLC | ||
| 48 | 00857834006605 | OMC-007 | Odyssey Micro Catheter | HERAEUS MEDICAL COMPONENTS LLC | ||
| 49 | 00857545008073 | FG 00464-08 | SF7072-105-27-30 | SelectFlex II 072 Neurovascular Access System 105cm, 27cm Variable Stiffness, 30cm Coating | Armadillo | Q'APEL MEDICAL LLC |
| 50 | 00857545008066 | FG 00464-07 | SF7072-95-27-30 | SelectFlex II 072 Neurovascular Access System 95cm, 27cm Variable Stiffness, 30cm Coating | Armadillo | Q'APEL MEDICAL LLC |