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 | 07613327519389 | INC-11814-160 | INC-11814-160 | Intermediate Catheter | AXS VECTA 46 | STRYKER CORPORATION |
2 | 07613327519372 | INC-11814-153 | INC-11814-153 | Intermediate Catheter | AXS VECTA 46 | STRYKER CORPORATION |
3 | 07613327519365 | INC-11814-146 | INC-11814-146 | Intermediate Catheter | AXS VECTA 46 | STRYKER CORPORATION |
4 | 07613327519358 | INC-11814-125 | INC-11814-125 | Intermediate Catheter | AXS VECTA 46 | STRYKER CORPORATION |
5 | 07613327459296 | INC-11648 | INC-11648 | Cliq Aspirator | VC-701 | STRYKER CORPORATION |
6 | 07613327459289 | INC-11790 | INC-11790 | Canister Set | Canister Set | STRYKER CORPORATION |
7 | 07613327459272 | INC-11460 | INC-11460 | Aspiration Tubing Set | Aspiration Tubing Set | STRYKER CORPORATION |
8 | 07613327459265 | INC-11597-132 | INC-11597-132 | Intermediate Catheter | AXS VECTA 74 | STRYKER CORPORATION |
9 | 07613327459258 | INC-11597-125 | INC-11597-125 | Intermediate Catheter | AXS VECTA 74 | STRYKER CORPORATION |
10 | 07613327459241 | INC-11597-115 | INC-11597-115 | Intermediate Catheter | AXS VECTA 74 | STRYKER CORPORATION |
11 | 07613327459234 | INC-11129-132 | INC-11129-132 | Intermediate Catheter | AXS VECTA 71 | STRYKER CORPORATION |
12 | 07613327459227 | INC-11129-125 | INC-11129-125 | Intermediate Catheter | AXS VECTA 71 | STRYKER CORPORATION |
13 | 07613327459210 | INC-11129-115 | INC-11129-115 | Intermediate Catheter | AXS VECTA 71 | STRYKER CORPORATION |
14 | 07613327417227 | IC068132 | IC068132 | Distal Access Catheter | AXS Catalyst 7 | STRYKER CORPORATION |
15 | 07613327417210 | IC068125 | IC068125 | Distal Access Catheter | AXS Catalyst 7 | STRYKER CORPORATION |
16 | 07613327417203 | IC068115 | IC068115 | Distal Access Catheter | AXS Catalyst 7 | STRYKER CORPORATION |
17 | 07613327299953 | 90315 | 90315 | ProVue Retriever | Trevo NXT | STRYKER CORPORATION |
18 | 07613327299946 | 90314 | 90314 | ProVue Retriever | Trevo NXT | STRYKER CORPORATION |
19 | 07613327299939 | 90313 | 90313 | ProVue Retriever | Trevo NXT | STRYKER CORPORATION |
20 | 07613327299922 | 90312 | 90312 | ProVue Retriever | Trevo NXT | STRYKER CORPORATION |
21 | 07613327012033 | M003IC0601320 | IC060132 | Distal Access Catheter | AXS Catalyst 6 | STRYKER CORPORATION |
22 | 07613327012019 | M003IC0581150 | IC058115 | Distal Access Catheter | AXS Catalyst 5 | STRYKER CORPORATION |
23 | 07613327011999 | M003IC0581320 | IC058132 | Distal Access Catheter | AXS Catalyst 5 | STRYKER CORPORATION |
24 | 07290015107303 | TRPP7144 | TRPP7144 | The Tigertriever 13 device is a stentriever that is comprised of an adjustable n The Tigertriever 13 device is a stentriever that is comprised of an adjustable nitinol braided mesh, stainless steel shaft, nitinol core wire and a handle. The shaft connects the mesh and the handle by the core wire that runs inside the shaft from the distal end of the mesh to the slider activation element in the handle. The mesh is expanded when the physician pulls the slider, since the wires of the mesh are completely radiopaque, the physician sees the mesh under fluoroscopy and controls it until it conforms to the vessel diameter. The design of the wire mesh is optimized to penetrate the clot and encapsulate it during retrieval. The Tigertriever 13 Revascularization Device is supplied sterile and is intended for single-use only by physicians trained in neuro-interventional catheterization and the treatment of ischemic stroke. | Tigertriever 13 Revascularization Device | RAPID MEDICAL LTD |
25 | 07290015107273 | TRPP7166 | The Tigertriever device is a stentriever that is comprised of an adjustable niti The Tigertriever device is a stentriever that is comprised of an adjustable nitinol braided mesh, stainless steel shaft, nitinol core wire and a handle. The shaft connects the mesh and the handle by the core wire that runs inside the shaft from the distal end of the mesh to the slider activation element in the handle. The mesh is expanded when the physician pulls the slider, since the wires of the mesh are completely radiopaque, the physician sees the mesh under fluoroscopy and controls it until it conforms to the vessel diameter. The design of the wire mesh is optimized to penetrate the clot and encapsulate it during retrieval. Two versions of the device are available. The standard version Tigertriever (TRPP7155) has a net length of 32mm (unexpanded form) and it is delivered through a microcatheter with an internal diameter of 0.021 inches. The shorter version Tigertriever 17 (TRPP7166) has a net length of 23 mm (unexpanded form) and it is delivered through a microcatheter with an internal diameter of 0.017 inches. The Tigertriever is provided with a 3.5 Fr peelable loading sheath. | Tigertriever 17 Revascularization Device | RAPID MEDICAL LTD | |
26 | 07290015107266 | TRPP7155 | TRPP7155 | The Tigertriever device is a stentriever that is comprised of an adjustable niti The Tigertriever device is a stentriever that is comprised of an adjustable nitinol braided mesh, stainless steel shaft, nitinol core wire and a handle. The shaft connects the mesh and the handle by the core wire that runs inside the shaft from the distal end of the mesh to the slider activation element in the handle. The mesh is expanded when the physician pulls the slider, since the wires of the mesh are completely radiopaque, the physician sees the mesh under fluoroscopy and controls it until it conforms to the vessel diameter. The design of the wire mesh is optimized to penetrate the clot and encapsulate it during retrieval. Two versions of the device are available. The standard version Tigertriever (TRPP7155) has a net length of 32mm (unexpanded form) and it is delivered through a microcatheter with an internal diameter of 0.021 inches. The shorter version Tigertriever 17 (TRPP7166) has a net length of 23 mm (unexpanded form) and it is delivered through a microcatheter with an internal diameter of 0.017 inches. The Tigertriever is provided with a 3.5 Fr peelable loading sheath. | Tigertriever Revascularization Device | RAPID MEDICAL LTD |
27 | 06970908211874 | ASP5F115KIT | Thrombectomy suction catheter | Esperance | SHANGHAI WALLABY MEDICAL TECHNOLOGIES CO., INC. | |
28 | 06970908211867 | ASP5F125KIT | Thrombectomy suction catheter | Esperance | SHANGHAI WALLABY MEDICAL TECHNOLOGIES CO., INC. | |
29 | 06970908211850 | ASP5F131KIT | Thrombectomy suction catheter | Esperance | SHANGHAI WALLABY MEDICAL TECHNOLOGIES CO., INC. | |
30 | 06970908211133 | ASP6F115KIT | Thrombectomy suction catheter | Esperance | SHANGHAI WALLABY MEDICAL TECHNOLOGIES CO., INC. | |
31 | 06970908211126 | ASP6F125KIT | Thrombectomy suction catheter | Esperance | SHANGHAI WALLABY MEDICAL TECHNOLOGIES CO., INC. | |
32 | 06970908211119 | ASP6F131KIT | Thrombectomy suction catheter | Esperance | SHANGHAI WALLABY MEDICAL TECHNOLOGIES CO., INC. | |
33 | 04719876940087 | AFT117B | ZOOM POD Aspiration Tubing, AFT117B | ZOOM Aspiration Pump | TAIWAN BIOMATERIAL COMPANY LIMITED | |
34 | 04719876940001 | TAT102B | ZOOM Aspiration Tubing, TAT102B | ZOOM Aspiration Pump | TAIWAN BIOMATERIAL COMPANY LIMITED | |
35 | 00847536044197 | REACT-71 | CATHETER REACT-71 V03 eIFU | REACT™ | MICRO THERAPEUTICS, INC. | |
36 | 00847536041967 | REACT-68 | CATHETER REACT-68 V03 eIFU | REACT™ | MICRO THERAPEUTICS, INC. | |
37 | 00847536034839 | MAT-110-110 | TUBING MAT-110-110 V01 | Riptide™ | MICRO THERAPEUTICS, INC. | |
38 | 00847536034792 | SFR3-6-40-10 | STENT SFR3-6-40-10 V06 ENHANCED | Solitaire™ Platinum | MICRO THERAPEUTICS, INC. | |
39 | 00847536034785 | SFR3-6-24-06 | STENT SFR3-6-24-06 V06 ENHANCED | Solitaire™ Platinum | MICRO THERAPEUTICS, INC. | |
40 | 00847536034778 | SFR3-6-20-10 | STENT SFR3-6-20-10 V06 ENHANCED | Solitaire™ Platinum | MICRO THERAPEUTICS, INC. | |
41 | 00847536034761 | SFR3-4-40-10 | STENT SFR3-4-40-10 V06 ENHANCED | Solitaire™ Platinum | MICRO THERAPEUTICS, INC. | |
42 | 00847536034754 | SFR3-4-20-10 | STENT SFR3-4-20-10 V06 ENHANCED | Solitaire™ Platinum | MICRO THERAPEUTICS, INC. | |
43 | 00847536034747 | SFR3-4-20-05 | STENT SFR3-4-20-05 V06 ENHANCED | Solitaire™ Platinum | MICRO THERAPEUTICS, INC. | |
44 | 00847536034730 | SFR4-6-40-10 | STENT SFR4-6-40-10 V01 US | Solitaire™ X | MICRO THERAPEUTICS, INC. | |
45 | 00847536034723 | SFR4-6-24-06 | STENT SFR4-6-24-06 V01 US | Solitaire™ X | MICRO THERAPEUTICS, INC. | |
46 | 00847536034716 | SFR4-6-20-10 | STENT SFR4-6-20-10 V01 US | Solitaire™ X | MICRO THERAPEUTICS, INC. | |
47 | 00847536034709 | SFR4-4-40-10 | STENT SFR4-4-40-10 V01 US | Solitaire™ X | MICRO THERAPEUTICS, INC. | |
48 | 00847536034693 | SFR4-4-20-10 | STENT SFR4-4-20-10 V01 US | Solitaire™ X | MICRO THERAPEUTICS, INC. | |
49 | 00847536034686 | SFR4-4-20-05 | STENT SFR4-4-20-05 V01 US | Solitaire™ X | MICRO THERAPEUTICS, INC. | |
50 | 00847536034044 | SFR3-6-40-10 | STENT SFR3-6-40-10 V05 EXTENDED IFU | Solitaire™ | MICRO THERAPEUTICS, INC. |