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 | 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 |
2 | 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 |
3 | 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 |
4 | 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 |
5 | 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 |
6 | 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 |
7 | 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 |
8 | 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 |
9 | 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 |
10 | 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 |
11 | 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 |
12 | 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 |
13 | 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 |
14 | 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 |
15 | 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 |
16 | 00851566003925 | VIA-17-154-01 | FGA17154-01 | VIA 17 Microcatheter | VIA Microcatheter | SEQUENT MEDICAL, INC. |
17 | 00851566003918 | VIA-21-154-01 | FGA21154-01 | VIA 21 Microcatheter | VIA Microcatheter | SEQUENT MEDICAL, INC. |
18 | 00851566003703 | VIA-33-133-01 | FG33133-01 | VIA 33 Microcatheter | VIA Microcatheter | SEQUENT MEDICAL, INC. |
19 | 00851566003420 | VIA-27-154-01 | FG27154-01 | VIA 27 Microcatheter | VIA Microcatheter | SEQUENT MEDICAL, INC. |
20 | 00850291007192 | 11-102 | FlorTriever 2 Catheter, Medium, 12Fr, 120 cm | FlowTriever 2 Catheter, M | INARI MEDICAL INC | |
21 | 00850291007185 | 22-101 | Triever24 Catheter, 24 Fr, 90 cm, Gen4 | Triever 24 | INARI MEDICAL INC | |
22 | 00850291007079 | 21-101 | Triever20 Catheter, Gen 4 | Triever20 | INARI MEDICAL INC | |
23 | 00850005115069 | 7240 | 7240 | Bashir™ Plus Endovascular Catheter 7Fr, 12.5cm basket, 40.0cm Infusion | Bashir™ Plus Endovascular Catheter 7Fr, 12.5cm basket, 40.0cm Infusion | THROMBOLEX, INC. |
24 | 00850005115052 | 7230 | 7230 | Bashir™ Plus Endovascular Catheter 7Fr, 12.5cm basket, 30.0cm Infusion | Bashir™ Plus Endovascular Catheter 7Fr, 12.5cm basket, 30.0cm Infusion | THROMBOLEX, INC. |
25 | 00850005115045 | 7220 | 7220 | Bashir™ Plus Endovascular Catheter 7Fr, 12.5cm basket, 20.0cm Infusion | Bashir™ Plus Endovascular Catheter 7Fr, 12.5cm basket, 20.0cm Infusion | THROMBOLEX, INC. |
26 | 00850005115038 | 7210 | 7210 | Bashir™ Plus Endovascular Catheter 7Fr, 12.5cm basket, 10.0cm Infusion | Bashir™ Plus Endovascular Catheter 7Fr, 12.5cm basket, 10.0cm Infusion | THROMBOLEX, INC. |
27 | 00850005115021 | 7101 | 7101 | Bashir™ S-B Endovascular Catheter 7Fr, 10.0cm basket | Bashir™ S-B Endovascular Catheter 7Fr, 10.0cm basket | THROMBOLEX, INC. |
28 | 00850005115014 | 7200 | Bashir™ N-X Endovascular Catheter | THROMBOLEX, INC. | ||
29 | 00850005115007 | 7201 | Bashir™ Endovascular Catheter | THROMBOLEX, INC. | ||
30 | 00847536041950 | FG19135-1030-1S | CATHETER FG19135-1030-1S V04 | PhenomTM Plus Catheter | MICRO THERAPEUTICS, INC. | |
31 | 00847536041943 | FG19135-0615-1S | CATHETER FG19135-0615-1S V04 | PhenomTM Plus Catheter | MICRO THERAPEUTICS, INC. | |
32 | 00847536041936 | FG19120-1030-1S | CATHETER FG19120-1030-1S V04 | PhenomTM Plus Catheter | MICRO THERAPEUTICS, INC. | |
33 | 00847536041929 | FG19120-1015-1S | CATHETER FG19120-1015-1S V04 | PhenomTM Plus Catheter | MICRO THERAPEUTICS, INC. | |
34 | 00847536041912 | FG19120-0630-1S | CATHETER FG19120-0630-1S V04 | PhenomTM Plus Catheter | MICRO THERAPEUTICS, INC. | |
35 | 00847536041905 | FG19105-0630-1S | CATHETER FG19105-0630-1S V04 | PhenomTM Plus Catheter | MICRO THERAPEUTICS, INC. | |
36 | 00847536041899 | FG19105-0615-1S | CATHETER FG19105-0615-1S V04 | PhenomTM Plus Catheter | MICRO THERAPEUTICS, INC. | |
37 | 00847536041882 | FG15160-0615-1S | CATHETER FG15160-0615-1S V04 | PhenomTM 27 Catheter | MICRO THERAPEUTICS, INC. | |
38 | 00847536041875 | FG15150-0630-1S | CATHETER FG15150-0630-1S V04 | PhenomTM 27 Catheter | MICRO THERAPEUTICS, INC. | |
39 | 00847536041868 | FG15150-0615-1S | CATHETER FG15150-0615-1S V04 | PhenomTM 27 Catheter | MICRO THERAPEUTICS, INC. | |
40 | 00847536041851 | FG15135-0615-1S | CATHETER FG15135-0615-1S V04 | PhenomTM 27 Catheter | MICRO THERAPEUTICS, INC. | |
41 | 00847536041844 | FG13160-0615-1S | CATHETER FG13160-0615-1S V04 | PhenomTM 21 Catheter | MICRO THERAPEUTICS, INC. | |
42 | 00847536041837 | FG13150-1015-2S | CATHETER FG13150-1015-2S V04 | PhenomTM 21 Catheter | MICRO THERAPEUTICS, INC. | |
43 | 00847536041820 | FG13150-0615-2X | CATHETER FG13150-0615-2X V04 | PhenomTM 21 Catheter | MICRO THERAPEUTICS, INC. | |
44 | 00847536041813 | FG13150-0615-2S | CATHETER FG13150-0615-2S V04 | PhenomTM 21 Catheter | MICRO THERAPEUTICS, INC. | |
45 | 00847536041806 | FG13150-0615-2R | CATHETER FG13150-0615-2R V04 | PhenomTM 21 Catheter | MICRO THERAPEUTICS, INC. | |
46 | 00847536041790 | FG13150-0615-2J | CATHETER FG13150-0615-2J V04 | PhenomTM 21 Catheter | MICRO THERAPEUTICS, INC. | |
47 | 00847536041783 | FG11160-0615-2X | CATHETER FG11160-0615-2X V04 | PhenomTM 17 Catheter | MICRO THERAPEUTICS, INC. | |
48 | 00847536041776 | FG11160-0615-2S | CATHETER FG11160-0615-2S V04 | PhenomTM 17 Catheter | MICRO THERAPEUTICS, INC. | |
49 | 00847536041769 | FG11160-0615-2R | CATHETER FG11160-0615-2R V04 | PhenomTM 17 Catheter | MICRO THERAPEUTICS, INC. | |
50 | 00847536041752 | FG11160-0615-2J | CATHETER FG11160-0615-2J V04 | PhenomTM 17 Catheter | MICRO THERAPEUTICS, INC. |