Other products from "MICRO THERAPEUTICS, INC."
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
Other products with the same Product Code "DQX"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 07640142811886 80239 80239 Rotational Excisional Atherectomy System. The Catheter Set includes one Rotarex™ Rotational Excisional Atherectomy System. The Catheter Set includes one Rotarex™S catheter (gauge 8F; length 110 cm), one guidewire (0.018” diameter; 270cm in length), one drape and one collecting bag. SET Rotarex™S 8 F x 110 cm STRAUB MEDICAL AG
2 07640142811879 80238 80238 Rotational Excisional Atherectomy System. The Catheter Set includes one Rotarex™ Rotational Excisional Atherectomy System. The Catheter Set includes one Rotarex™S catheter (gauge 8F; length 85 cm), one guidewire (0.018” diameter; 220cm in length), one drape and one collecting bag. SET Rotarex™S 8 F x 85 cm STRAUB MEDICAL AG
3 07640142811862 80237 80237 Rotational Excisional Atherectomy System. The Catheter Set includes one Rotarex™ Rotational Excisional Atherectomy System. The Catheter Set includes one Rotarex™S catheter (gauge 6F; length 135 cm), one guidewire (0.018” diameter; 320 cm in length), one sterile and one collecting bag. SET Rotarex™S 6 F x 135 cm STRAUB MEDICAL AG
4 07640142811855 80236 80236 Rotational Excisional Atherectomy System. The Catheter Set includes one Rotarex™ Rotational Excisional Atherectomy System. The Catheter Set includes one Rotarex™S catheter (gauge 6F ; length 110 cm), one guidewire (0.018” diameter; 270cm in length), one drape and one collecting bag. SET Rotarex™S 6 F x 110 cm STRAUB MEDICAL AG
5 07640142811350 80328 80328 The Aspirex™ Thrombectomy Catheter Set is composed of one Aspirex™ Thrombectomy The Aspirex™ Thrombectomy Catheter Set is composed of one Aspirex™ Thrombectomy Catheter (gauge 10F; length 110cm), one Aspirex™ Guidewire (0.025” diameter; 270cm in length), one collecting bag, and one sterile drape. SET Aspirex™ S 10F 110cm STRAUB MEDICAL AG
6 07640142811343 80327 80327 The Aspirex™ Thrombectomy Catheter Set is composed of one Aspirex™ Thrombectomy The Aspirex™ Thrombectomy Catheter Set is composed of one Aspirex™ Thrombectomy Catheter (gauge 8F; length 110cm), one Aspirex™ Guidewire (0.018” diameter; 270cm in length), one collecting bag, and one sterile drape. SET Aspirex™ S 8F 110cm STRAUB MEDICAL AG
7 07640142811336 80326 80326 The Aspirex™ Thrombectomy Catheter Set is composed of one Aspirex™ Thrombectomy The Aspirex™ Thrombectomy Catheter Set is composed of one Aspirex™ Thrombectomy Catheter (gauge 8F; length 85cm), one Aspirex™ Guidewire (0.018” diameter; 220cm in length), one collecting bag, and one sterile drape. SET Aspirex™ S 8F 85cm STRAUB MEDICAL AG
8 07640142811329 80325 80325 The Aspirex™ Thrombectomy Catheter Set is composed of one Aspirex™ Thrombectomy The Aspirex™ Thrombectomy Catheter Set is composed of one Aspirex™ Thrombectomy Catheter (gauge 6F; length 135cm), one Aspirex™ Guidewire (0.018” diameter; 320 cm in length), one collecting bag, and one sterile drape. SET Aspirex™ S 6F 135cm STRAUB MEDICAL AG
9 07640142811312 80324 80324 The Aspirex™ S Thrombectomy Catheter Set is composed of one Aspirex™ S Thrombect The Aspirex™ S Thrombectomy Catheter Set is composed of one Aspirex™ S Thrombectomy Catheter (gauge 6F; length 110cm), one Aspirex™ S Guidewire (0.018” diameter; 270cm in length), one collecting bag, and one sterile drape. SET Aspirex™ S 6F 110cm STRAUB MEDICAL AG
10 07640142811305 80256 80256 The Rotarex™ S and Aspirex™ S Guidewire has a LubriSkin PTFE-coated nitinol core The Rotarex™ S and Aspirex™ S Guidewire has a LubriSkin PTFE-coated nitinol core wire with a gold-plated Tungsten tip coated with DSM ComfortCoat® hydrophilic coating. The guidewire is used to initially cross through the area to be treated. To be used with Straub Medical catheters. Guidewire 0.025 6/270cm angled STRAUB MEDICAL AG
11 07640142810605 Version 1.0 80239 Rotational Excisional Atherectomy System.The Catheter Set includes one Rotarex®S Rotational Excisional Atherectomy System.The Catheter Set includes one Rotarex®S catheter (gauge 8F; length 110 cm), one guidewire (0.018” diameter; 270cm in length), one drape and one collecting bag. SET Rotarex®S 8F 110 cm (Straub Medical®) STRAUB MEDICAL AG
12 07640142810599 Version 1.0 80238 Rotational Excisional Atherectomy System.The Catheter Set includes one Rotarex®S Rotational Excisional Atherectomy System.The Catheter Set includes one Rotarex®S catheter (gauge 8F; length 85 cm), one guidewire (0.018” diameter; 220cm in length), one drape and one collecting bag. SET Rotarex®S 8F 85cm (Straub Medical®) STRAUB MEDICAL AG
13 07640142810582 Version 1.0 80237 Rotational Excisional Atherectomy System. The Catheter Set includes one Rotarex® Rotational Excisional Atherectomy System. The Catheter Set includes one Rotarex®S catheter (gauge 6F; length 135 cm), one guidewire (0.018” diameter; 320 cm in length), one drape and one collecting bag. SET Rotarex®S 6F 135cm (Straub Medical®) STRAUB MEDICAL AG
14 07640142810575 Version 1.0 80236 Rotational Excisional Atherectomy System.The Catheter Set includes one Rotarex®S Rotational Excisional Atherectomy System.The Catheter Set includes one Rotarex®S catheter (gauge 6F; length 110 cm), one guidewire (0.018” diameter; 270cm in length), one drape and one collecting bag. SET Rotarex®S 6F 110cm (Straub Medical®) STRAUB MEDICAL AG
15 07640142810261 Version 1.0 80235 The Rotarex™ S and Aspirex™ S Guidewire has a LubriSkin PTFE-coated nitinol core The Rotarex™ S and Aspirex™ S Guidewire has a LubriSkin PTFE-coated nitinol core wire with a gold-plated Tungsten tip coated with DSM ComfortCoat® hydrophilic coating. The guidewire is used to initially cross through the area to be treated. To be used with Straub Medical catheters. Guidewire 0.018 4/320cm angled (Straub Medical®) STRAUB MEDICAL AG
16 07640142810254 Version 1.0 80234 The Rotarex™ S and Aspirex™ S Guidewire has a LubriSkin PTFE-coated nitinol core The Rotarex™ S and Aspirex™ S Guidewire has a LubriSkin PTFE-coated nitinol core wire with a gold-plated Tungsten tip coated with DSM ComfortCoat® hydrophilic coating. The guidewire is used to initially cross through the area to be treated. To be used with Straub Medical catheters. Guidewire 0.018 4/270cm angled (Straub Medical®) STRAUB MEDICAL AG
17 07640142810247 Version 1.0 80233 The Rotarex™ S and Aspirex™ S Guidewire has a LubriSkin PTFE-coated nitinol core The Rotarex™ S and Aspirex™ S Guidewire has a LubriSkin PTFE-coated nitinol core wire with a gold-plated Tungsten tip coated with DSM ComfortCoat® hydrophilic coating. The guidewire is used to initially cross through the area to be treated. To be used with Straub Medical catheters. Guidewire 0.018 4/220cm angled (Straub Medical®) STRAUB MEDICAL AG
18 07640130442733 Stiff 300cm 357262 Cruiser-18 BIOTRONIK AG
19 07640130442726 Medium 300cm 357261 Cruiser-18 BIOTRONIK AG
20 07640130442719 Stiff 195cm 357260 Cruiser-18 BIOTRONIK AG
21 07640130442702 Medium 195cm 357259 Cruiser-18 BIOTRONIK AG
22 07613327508642 SSUP300PRE SSUP300PRE SUPPORT PRE-SHAPED Guidewire with Hydrophilic Coating Synchro SELECT STRYKER CORPORATION
23 07613327508635 SSUP215PRE SSUP215PRE SUPPORT PRE-SHAPED Guidewire with Hydrophilic Coating Synchro SELECT STRYKER CORPORATION
24 07613327508628 SSUP300STR SSUP300STR SUPPORT STRAIGHT Guidewire with Hydrophilic Coating Synchro SELECT STRYKER CORPORATION
25 07613327508611 SSUP215STR SSUP215STR SUPPORT STRAIGHT Guidewire with Hydrophilic Coating Synchro SELECT STRYKER CORPORATION
26 07613327508604 SSFT300PRE SSFT300PRE SOFT PRE-SHAPED Guidewire with Hydrophilic Coating Synchro SELECT STRYKER CORPORATION
27 07613327508598 SSFT215PRE SSFT215PRE SOFT PRE-SHAPED Guidewire with Hydrophilic Coating Synchro SELECT STRYKER CORPORATION
28 07613327508581 SSFT300STR SSFT300STR SOFT STRAIGHT Guidewire with Hydrophilic Coating Synchro SELECT STRYKER CORPORATION
29 07613327508574 SSFT215STR SSFT215STR SOFT STRAIGHT Guidewire with Hydrophilic Coating Synchro SELECT STRYKER CORPORATION
30 07613327508529 SSTD300PRE SSTD300PRE STANDARD PRE-SHAPED Guidewire with Hydrophilic Coating Synchro SELECT STRYKER CORPORATION
31 07613327508512 SSTD215PRE SSTD215PRE STANDARD PRE-SHAPED Guidewire with Hydrophilic Coating Synchro SELECT STRYKER CORPORATION
32 07613327508505 SSTD300STR SSTD300STR STANDARD STRAIGHT Guidewire with Hydrophilic Coating Synchro SELECT STRYKER CORPORATION
33 07613327508499 SSTD215STR SSTD215STR STANDARD STRAIGHT Guidewire with Hydrophilic Coating Synchro SELECT STRYKER CORPORATION
34 07613327459661 S2SPP14300 S2SPP14300 SUPPORT PRE-SHAPED Guidewire with Hydrophilic Coating Synchro2 STRYKER CORPORATION
35 07613327459654 S2SPP14215 S2SPP14215 SUPPORT PRE-SHAPED Guidewire with Hydrophilic Coating Synchro2 STRYKER CORPORATION
36 07613327459647 S2SPS14300 S2SPS14300 SUPPORT Guidewire with Hydrophilic Coating Synchro2 STRYKER CORPORATION
37 07613327459630 S2SPS14215 S2SPS14215 SUPPORT Guidewire with Hydrophilic Coating Synchro2 STRYKER CORPORATION
38 H965970001030 97000103 Angiographic Guidewire, Fixed Core, Straight Tip Navilyst NAVILYST MEDICAL, INC.
39 H965970001020 97000102 Angiographic Guidewire, Fixed Core, Straight Tip Navilyst NAVILYST MEDICAL, INC.
40 H965970001010 97000101 Angiographic Guidewire, Fixed Core, Straight Tip Navilyst NAVILYST MEDICAL, INC.
41 H965970006020 97000602 Angiographic Guidewire, Fixed Core, Straight Tip Navilyst NAVILYST MEDICAL, INC.
42 H965970006010 97000601 Angiographic Guidewire, Fixed Core, Straight Tip Navilyst NAVILYST MEDICAL, INC.
43 H965970005080 97000508 Angiographic Guidewire, Movable Core, J Tip Navilyst NAVILYST MEDICAL, INC.
44 H965970005070 97000507 Angiographic Guidewire, Movable Core, J Tip Navilyst NAVILYST MEDICAL, INC.
45 H965970005050 97000505 Angiographic Guidewire, Movable Core, J Tip Navilyst NAVILYST MEDICAL, INC.
46 H965970005040 97000504 Angiographic Guidewire, Movable Core, J Tip Navilyst NAVILYST MEDICAL, INC.
47 H965970005030 97000503 Angiographic Guidewire, Movable Core, J Tip Navilyst NAVILYST MEDICAL, INC.
48 H965970005010 97000501 Angiographic Guidewire, Movable Core, J Tip Navilyst NAVILYST MEDICAL, INC.
49 H965970004060 97000406 Angiographic Guidewire, Fixed Core, J Tip Navilyst NAVILYST MEDICAL, INC.
50 H965970004050 97000405 Angiographic Guidewire, Fixed Core, J Tip Navilyst NAVILYST MEDICAL, INC.