No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00763000500993 | BB11N31R1 | CUSTOM PACK BB11N31R1 RESEARCH PACK | DWF | Catheter, cannula and tubing, vascular, cardiopulmonary bypass | 2 | NA | |
2 | 00763000500979 | BB11N23R | CUSTOM PACK BB11N23R 10PK XTRASUC | DWF | Catheter, cannula and tubing, vascular, cardiopulmonary bypass | 2 | NA | |
3 | 00763000500962 | BB10R11R5 | CUSTOM PACK BB10R11R5 PUMP PK | DWF | Catheter, cannula and tubing, vascular, cardiopulmonary bypass | 2 | NA | |
4 | 00763000500948 | BB5Z34R5 | CUSTOM PACK BB5Z34R5 NURSES | DWF | Catheter, cannula and tubing, vascular, cardiopulmonary bypass | 2 | NA | |
5 | 00763000500931 | BB11G46R1 | CUSTOM PACK BB11G46R1 RQST2 | DWF | Catheter, cannula and tubing, vascular, cardiopulmonary bypass | 2 | NA | |
6 | 00763000500634 | 7H97R2 | CUSTOM PACK 7H97R2 25PK FEMALE ADAPT | DWF | Catheter, cannula and tubing, vascular, cardiopulmonary bypass | 2 | NA | |
7 | 00763000500559 | HY10Z01R8 | CUSTOM PACK HY10Z01R8 SUPPORT PACK | DWF | Catheter, cannula and tubing, vascular, cardiopulmonary bypass | 2 | NA | |
8 | 00763000501105 | BB5B82R2 | CUSTOM PACK BB5B82R2 5PK SUPPLE 2 | DWF | Catheter, cannula and tubing, vascular, cardiopulmonary bypass | 2 | NA | |
9 | 00763000511555 | ONYXNG35012UX | STENT ONYXNG35012UX ONYX 3.50X12RX | NIQ | Coronary drug-eluting stent | 3 | Onyx Frontier™ | |
10 | 00763000498535 | BB11L44R2 | CUSTOM PACK BB11L44R2 OPEN HEART | DWF | Catheter, cannula and tubing, vascular, cardiopulmonary bypass | 2 | NA | |
11 | 00763000511470 | ONYXNG30015UX | STENT ONYXNG30015UX ONYX 3.00X15RX | NIQ | Coronary drug-eluting stent | 3 | Onyx Frontier™ | |
12 | 00763000511418 | ONYXNG27526UX | STENT ONYXNG27526UX ONYX 2.75X26RX | NIQ | Coronary drug-eluting stent | 3 | Onyx Frontier™ | |
13 | 00763000511326 | ONYXNG25026UX | STENT ONYXNG25026UX ONYX 2.50X26RX | NIQ | Coronary drug-eluting stent | 3 | Onyx Frontier™ | |
14 | 00763000489472 | HY7Y30R18 | CUSTOM PACK HY7Y30R18 EC AMBU | DWF | Catheter, cannula and tubing, vascular, cardiopulmonary bypass | 2 | NA | |
15 | 00763000489434 | BB7L75R3 | CUSTOM PACK BB7L75R3 10PK 3/8X 72 | DWF | Catheter, cannula and tubing, vascular, cardiopulmonary bypass | 2 | NA | |
16 | 00763000426422 | B3301533M | LEAD B3301533M SENSIGHT 1.5MM EMAN LJ53 | MHY,MRU,NHL,PJS,MBX | Stimulator, electrical, implanted, for parkinsonian tremor,implanted subcortical Stimulator, electrical, implanted, for parkinsonian tremor,implanted subcortical electrical Stimulator (motor disorders),Stimulator, electrical, implanted, for parkinsonian symptoms,Stimulator, electrical, implanted, for essential tremor,Stimulator, thalamic, epilepsy, implanted | 3 | SenSight™ | |
17 | 00763000426408 | B3300542M | LEAD B3300542M SENSIGHT 0.5MM EMAN LJ53 | MBX,NHL,MRU,PJS,MHY | Stimulator, thalamic, epilepsy, implanted,Stimulator, electrical, implanted, for Stimulator, thalamic, epilepsy, implanted,Stimulator, electrical, implanted, for parkinsonian symptoms,implanted subcortical electrical Stimulator (motor disorders),Stimulator, electrical, implanted, for essential tremor,Stimulator, electrical, implanted, for parkinsonian tremor | 3 | SenSight™ | |
18 | 00763000334178 | 11D35R | CUSTOM PACK 11D35R RETO5 | DWF | Catheter, cannula and tubing, vascular, cardiopulmonary bypass | 2 | NA | |
19 | 00763000334130 | 11D33R | CUSTOM PACK 11D33R RETO1 | DWF | Catheter, cannula and tubing, vascular, cardiopulmonary bypass | 2 | NA | |
20 | 00763000306144 | ETBF3216C166E | STENT GRAFT ETBF3216C166E ENDUR II BIF | MIH | SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT | 3 | Endurant® II | |
21 | 00763000305659 | ETLW1624C93E | STENT GRAFT ETLW1624C93E ENDUR II LIMB | MIH | SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT | 3 | Endurant® II | |
22 | 00763000305598 | ETLW1620C82E | STENT GRAFT ETLW1620C82E ENDUR II LIMB | MIH | SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT | 3 | Endurant® II | |
23 | 00763000271220 | 7800RR36 | RING 7800RR36 SIMUFORM SR 36MM US | KRH | RING, ANNULOPLASTY | 2 | SimuForm™ | |
24 | 00763000271107 | 7700FR32 | RING 7700FR32 SIMUPLUS FLEX 32MM US | KRH | RING, ANNULOPLASTY | 2 | SimuPlus™ | |
25 | 00763000499945 | BB5U74R18 | CUSTOM PACK BB5U74R18 TUBING | DWF | Catheter, cannula and tubing, vascular, cardiopulmonary bypass | 2 | NA | |
26 | 00763000499921 | BB8S37R29 | CUSTOM PACK BB8S37R29 PUMP TBL | DWF | Catheter, cannula and tubing, vascular, cardiopulmonary bypass | 2 | NA | |
27 | 00763000511647 | ONYXNG40012UX | STENT ONYXNG40012UX ONYX 4.00X12RX | NIQ | Coronary drug-eluting stent | 3 | Onyx Frontier™ | |
28 | 00763000498870 | CB11N89R | CUSTOM PACK CB11N89R MAN/BRIDGE | DWF | Catheter, cannula and tubing, vascular, cardiopulmonary bypass | 2 | NA | |
29 | 00763000260743 | VNMC2828C90TU | STENT GRAFT VNMC2828C90TU VAL NAV CS | MIH | SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT | 3 | Valiant Navion™ | |
30 | 00763000001377 | BB8B73R7 | CUSTOM PACK BB8B73R7 PK | DWE | TUBING, PUMP, CARDIOPULMONARY BYPASS | 2 | NA | |
31 | 00681490024273 | 05328 | CABLE 05328 ATAKR EGM SAFETY 8FT | LPB | Cardiac ablation percutaneous catheter | 3 | NA | |
32 | 00673978549071 | 5344 | PLUG 5344 1/4 INCH | DWE | TUBING, PUMP, CARDIOPULMONARY BYPASS | 2 | NA | |
33 | 00643169796454 | AB9U20100090 | STENT AB9U20100090 ABRE V01 | QAN | Stent, iliac vein | 3 | Abre™ | |
34 | 00643169518919 | 97740 | PROG 97740 PATIENT MRICS SCS USA ROHS | LGW | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF | 3 | NA | |
35 | 00643169078024 | 500FA27 | MHV 500FA27 STD AORTIC | LWQ | HEART-VALVE, MECHANICAL | 3 | Open Pivot™ | |
36 | 00613994759221 | 680R32 | RING 680R32 PROFILE 3D 26L MEXICO | KRH | RING, ANNULOPLASTY | 2 | PROFILE 3D® | |
37 | 00613994691392 | 37642 | PRGMR 37642 PATIENT DBS W SC,PC,RC | MFR,NHL,MHY,OLM,MRU | Stimulator, brain, implanted, for behavior modification,STIMULATOR, ELECTRICAL, Stimulator, brain, implanted, for behavior modification,STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN SYMPTOMS,STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR,Deep brain stimulator for obsessive compulsive disorder (OCD),implanted subcortical electrical Stimulator (motor disorders) | 3 | NA | |
38 | 00613994334565 | 68005YN | CABLE 68005YN EGM 18L | OCL | Surgical Device, For cutting, coagulation, and/or ablation of tissue, including Surgical Device, For cutting, coagulation, and/or ablation of tissue, including cardiac tissue | 2 | NA | |
39 | 00885074469669 | 365538 | TUNNEL TOOL 365538 ACCESSORY KIT US MKT | HAO | INSTRUMENT, SURGICAL, NON-POWERED | 1 | NA | |
40 | 00885074375458 | SB7MAC30 | CATHETER SB7MAC30 SB 7F 100CM MA30 | DQY | CATHETER, PERCUTANEOUS | 2 | SHERPA NX BALANCED | |
41 | 00885074372181 | SB7EBU40D | CATHETER SB7EBU40D SB 7F 90CM EB40 | DQY | CATHETER, PERCUTANEOUS | 2 | SHERPA NX BALANCED | |
42 | 00763000665982 | BB11V67R3 | CUSTOM PACK BB11V67R3 UMC | DWF | Catheter, cannula and tubing, vascular, cardiopulmonary bypass | 2 | NA | |
43 | 00763000552985 | CB11J56R3 | CUSTOM PACK CB11J56R3 PEDI MAG | DWF | Catheter, cannula and tubing, vascular, cardiopulmonary bypass | 2 | NA | |
44 | 00763000541118 | 6A32R2 | CUSTOM PACK 6A32R2 1/4X1/4 | DWF | Catheter, cannula and tubing, vascular, cardiopulmonary bypass | 2 | NA | |
45 | 00763000400866 | 3320L | LIT 3320L DYSTONIA EMANUALS EN | MRU | implanted subcortical electrical Stimulator (motor disorders) | N/A | ||
46 | 00763000502843 | FMET-IM-SYS-S | SYSTEM SERVICED FMET-IM-SYS-S | DPW | FLOWMETER, BLOOD, CARDIOVASCULAR | 2 | FlowMet™ | |
47 | 00763000390891 | LA6ERADRST | CATHETER LA6ERADRST LA 6F 100CM ERDRS | DQY | Catheter, percutaneous | 2 | Launcher | |
48 | 00763000310332 | 37601 | INS 37601 ACTIVA PC DBS EMANUAL EN | OLM,MRU,MHY,NHL,MBX,PJS | Deep brain stimulator for obsessive compulsive disorder (OCD),implanted subcorti Deep brain stimulator for obsessive compulsive disorder (OCD),implanted subcortical electrical Stimulator (motor disorders),STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR,Stimulator, electrical, implanted, for parkinsonian symptoms,STIMULATOR, THALAMIC, EPILEPSY, IMPLANTED,Stimulator, electrical, implanted, for essential tremor | 3 | Activa® PC | |
49 | 00763000306519 | 104FS | FOOTSWITCH 104FS CRYOCONSOLE MDR | LPB | Cardiac ablation percutaneous catheter | 3 | N/A | |
50 | 00763000301330 | HC150A | HANDCRANK HC150A PLX 31L | DWA | Control, pump speed, cardiopulmonary bypass | 2 | Affinity™ |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 00851354004189 | O200 | O200 | The Ocelot System is intended to facilitate the intraluminal placement of conven The Ocelot System is intended to facilitate the intraluminal placement of conventional guidewires beyond stenotic lesions (including sub and chronic total occlusions) in the peripheral vasculature prior to further percutaneous intervention using OCT-assisted orientation and imaging. The system is an adjunct to fluoroscopy by providing images of vessel lumen and wall structures. The Ocelot System is contraindicated for use in the iliac, coronary, cerebral, renal or carotid vasculature. | Ocelot III | AVINGER, INC. |
2 | 00851354004073 | J100 | J100 | Juicebox is an optional accessory to facilitate catheter tip rotation when using Juicebox is an optional accessory to facilitate catheter tip rotation when using a compatible Avinger catheter. It consists of a handle with a Rotation Toggle Switch and a Release Button. Juicebox is designed to be placed over the catheter handle. This accessory is irradiated for sterility and is intended for single use only. When Juicebox is properly placed over a catheter handle, it locks into place. Depressing the Rotation Toggle Switch activates the power for rotation in either the clockwise or counterclockwise directions. The Release Button releases Juicebox so that it can be removed from the catheter handle.The Juicebox is an optional accessory that may be used to facilitate catheter tip rotation when using a compatible Avinger catheter. | Juicebox | AVINGER, INC. |
3 | 00851354004059 | E550 | E550 | "Kittycat 2 Catheter is a 5F sheath and 0.014” guidewire compatible over-the-wi "Kittycat 2 Catheter is a 5F sheath and 0.014” guidewire compatible over-the-wire device with a working length of 150 cm. It consists of a catheter shaft with handle assembly at the proximal end and an atraumatic Distal Tip. A locking Luer connecter at the proximal end provides entry to a lumen that supports and facilitates movement of a guidewire. The catheter has been irradiated for sterility and is intended for single use only.The Distal Tip houses Spiral Flutes and allows atraumatic advancement of the catheter through the vasculature. The pre-shaped Distal Tip is made of a malleable material and may be reshaped as needed by the user. The deflection of the Distal Tip is visible under fluoroscopic guidance.The handle assembly consists of a Handle Body, Rotator, and Luer. The Handle Body controls rotational orientation of the catheter, including the flexible Distal Tip. The Rotator controls the rotational movement of the Distal Tip, independent of the catheter orientation. The Luer is provided at the proximal end to facilitate fluid flush and the entry/exit of the guidewire. Kittycat 2 is intended to create a channel in totally occluded peripheral vessels. The device may also be used to facilitate the intraluminal placement of conventional guidewires beyond stenotic lesions (including sub and chronic total occlusions) in the peripheral vasculature prior to further percutaneous intervention. " | Kittykat II | AVINGER, INC. |
4 | 00851354004042 | W550` | W550 | "Kittycat 2 Catheter is a 5F sheath and 0.014” guidewire compatible over-the-wi "Kittycat 2 Catheter is a 5F sheath and 0.014” guidewire compatible over-the-wire device with a working length of 150 cm. It consists of a catheter shaft with handle assembly at the proximal end and an atraumatic Distal Tip. A locking Luer connecter at the proximal end provides entry to a lumen that supports and facilitates movement of a guidewire. The catheter has been irradiated for sterility and is intended for single use only.The Distal Tip houses Spiral Flutes and allows atraumatic advancement of the catheter through the vasculature. The pre-shaped Distal Tip is made of a malleable material and may be reshaped as needed by the user. The deflection of the Distal Tip is visible under fluoroscopic guidance.The handle assembly consists of a Handle Body, Rotator, and Luer. The Handle Body controls rotational orientation of the catheter, including the flexible Distal Tip. The Rotator controls the rotational movement of the Distal Tip, independent of the catheter orientation. The Luer is provided at the proximal end to facilitate fluid flush and the entry/exit of the guidewire. Kittycat 2 is intended to facilitate the intraluminal placement of conventional guidewires beyond stenotic lesions (including sub and chronic total occlusions) in the peripheral vasculature prior to further percutaneous intervention. The Kittycat 2 Catheter is contraindicated for use in the iliac, coronary, cerebral or carotid vasculature.Kittycat 2 is intended to be used to support steerable guidewires in accessing discrete regions of the peripheral vasculature. It may be used to facilitate placement and exchange of guidewires and other interventional devices. It may also be used to deliver saline or contrast." | Kittykat II | AVINGER, INC. |
5 | 00851354004028 | E400 | E400 | "The Wildcat CTO Catheter is intended to create a channel in totally occluded pe "The Wildcat CTO Catheter is intended to create a channel in totally occluded peripheral vessels. The device may also be used to faciliate the intraluminal placement of conventional guidewires beyond stenotic lesions (including sub and chronic total occlusions) in the peripheral vasculature prior to further percutaneous intervention. The Wildcat CTO Catheter is a 6F sheath and 0.035"" guidewire compatible over-the-wire device. It consists of a catheter shaft with a handle assembly at the porximal end and an atraumatic Distal Tip. A locking Luer connector at the proximal end provides entry to a lumen that supports and facilitates movement of a guidewire. The catheter has been irradiated for sterility and is intended for single use only. At the Slider’s most proximal location, the Wedges are in the retracted position. At the mid-point location, the Wedges are deployed. Moving the slider distal from this point initiates deflection of the Distal Tip. The amount of tip deflection increases with distal movement of the slider. At the most distal location, the Wedges remain fully deployed and the Distal Tip is at maximum deflection. The deployment and retraction of the Wedges as well as the deflection of the Distal Tip is visible under fluoroscopic guidance.The handle assembly consists of a Handle Body, Rotator, Tip Indicator, Slider, and Luer. The Handle Body controls rotational orientation of the catheter, including the flexible Distal Tip. The Rotator controls the rotational movement of the Distal Tip, independent of the catheter orientation. Rotational movement of the Distal Tip can be achieved either with Wedges deployed or retracted. Luer is provided to facilitate fluid flush and the entry/exit of the guidewire. " | Wildcat | AVINGER, INC. |
6 | 00851354004004 | W400 | W400 | "The Wildcat CTO Catheter is intended to create a channel in totally occluded pe "The Wildcat CTO Catheter is intended to create a channel in totally occluded peripheral vessels. The device may also be used to faciliate the intraluminal placement of conventional guidewires beyond stenotic lesions (including sub and chronic total occlusions) in the peripheral vasculature prior to further percutaneous intervention. The Wildcat Catheter is contraindicated for use in the iliac, coronary, cerebral or carotid vasculature. The Wildcat Catheter is intended to be used to support steerable guidewires in accessing discrete regions of the peripheral vasculature. It may be used to facilitate placement and exchange of guidewires and other interventional devices. It may also be used to deliver saline or contrast.The Wildcat CTO Catheter is a 6F sheath and 0.035"" guidewire compatible over-the-wire device. It consists of a catheter shaft with a handle assembly at the porximal end and an atraumatic Distal Tip. A locking Luer connector at the proximal end provides entry to a lumen that supports and facilitates movement of a guidewire. The catheter has been irradiated for sterility and is intended for single use only. At the Slider’s most proximal location, the Wedges are in the retracted position. At the mid-point location, the Wedges are deployed. Moving the slider distal from this point initiates deflection of the Distal Tip. The amount of tip deflection increases with distal movement of the slider. At the most distal location, the Wedges remain fully deployed and the Distal Tip is at maximum deflection. The deployment and retraction of the Wedges as well as the deflection of the Distal Tip is visible under fluoroscopic guidance. | Wildcat | AVINGER, INC. |
7 | 00850025525091 | SPN35150US | Spex Shapeable Support Catheter, 35 X 150cm, US | SPEX35 | REFLOW MEDICAL, INC. | |
8 | 00850025525084 | SPN35135US | Spex Shapeable Support Catheter, 35 X 135cm, US | SPEX35 | REFLOW MEDICAL, INC. | |
9 | 00850025525077 | SPN35090US | Spex Shapeable Support Catheter, 35 X 90cm, US | SPEX35 | REFLOW MEDICAL, INC. | |
10 | 00850025525060 | SPN35050US | Spex Shapeable Support Catheter, 35 X 50cm, US | SPEX35 | REFLOW MEDICAL, INC. | |
11 | 00850025525053 | CRX14150US | Cora Cross Coronary Crossing Catheter 14X150cm | coraCross | REFLOW MEDICAL, INC. | |
12 | 00850025525046 | CRX14135US | Cora Cross Coronary Crossing Catheter 14X135cm | coraCross | REFLOW MEDICAL, INC. | |
13 | 00850025525039 | SLP35150US | speX LP Shapeable Support Catheter, 35 X 150cm, US | Spex LP | REFLOW MEDICAL, INC. | |
14 | 00850025525022 | SLP35135US | speX LP Shapeable Support Catheter, 35 X 135cm, US | Spex LP | REFLOW MEDICAL, INC. | |
15 | 00850025525015 | SLP35090US | speX LP Shapeable Support Catheter, 35 X 90cm, US | Spex LP | REFLOW MEDICAL, INC. | |
16 | 00847536044197 | REACT-71 | CATHETER REACT-71 V03 eIFU | REACT™ | MICRO THERAPEUTICS, INC. | |
17 | 00847536041967 | REACT-68 | CATHETER REACT-68 V03 eIFU | REACT™ | MICRO THERAPEUTICS, INC. | |
18 | 00847536041950 | FG19135-1030-1S | CATHETER FG19135-1030-1S V04 | PhenomTM Plus Catheter | MICRO THERAPEUTICS, INC. | |
19 | 00847536041943 | FG19135-0615-1S | CATHETER FG19135-0615-1S V04 | PhenomTM Plus Catheter | MICRO THERAPEUTICS, INC. | |
20 | 00847536041936 | FG19120-1030-1S | CATHETER FG19120-1030-1S V04 | PhenomTM Plus Catheter | MICRO THERAPEUTICS, INC. | |
21 | 00847536041929 | FG19120-1015-1S | CATHETER FG19120-1015-1S V04 | PhenomTM Plus Catheter | MICRO THERAPEUTICS, INC. | |
22 | 00847536041912 | FG19120-0630-1S | CATHETER FG19120-0630-1S V04 | PhenomTM Plus Catheter | MICRO THERAPEUTICS, INC. | |
23 | 00847536041905 | FG19105-0630-1S | CATHETER FG19105-0630-1S V04 | PhenomTM Plus Catheter | MICRO THERAPEUTICS, INC. | |
24 | 00847536041899 | FG19105-0615-1S | CATHETER FG19105-0615-1S V04 | PhenomTM Plus Catheter | MICRO THERAPEUTICS, INC. | |
25 | 00847536041882 | FG15160-0615-1S | CATHETER FG15160-0615-1S V04 | PhenomTM 27 Catheter | MICRO THERAPEUTICS, INC. | |
26 | 00847536041875 | FG15150-0630-1S | CATHETER FG15150-0630-1S V04 | PhenomTM 27 Catheter | MICRO THERAPEUTICS, INC. | |
27 | 00847536041868 | FG15150-0615-1S | CATHETER FG15150-0615-1S V04 | PhenomTM 27 Catheter | MICRO THERAPEUTICS, INC. | |
28 | 00847536041851 | FG15135-0615-1S | CATHETER FG15135-0615-1S V04 | PhenomTM 27 Catheter | MICRO THERAPEUTICS, INC. | |
29 | 00847536041844 | FG13160-0615-1S | CATHETER FG13160-0615-1S V04 | PhenomTM 21 Catheter | MICRO THERAPEUTICS, INC. | |
30 | 00847536041837 | FG13150-1015-2S | CATHETER FG13150-1015-2S V04 | PhenomTM 21 Catheter | MICRO THERAPEUTICS, INC. | |
31 | 00847536041820 | FG13150-0615-2X | CATHETER FG13150-0615-2X V04 | PhenomTM 21 Catheter | MICRO THERAPEUTICS, INC. | |
32 | 00847536041813 | FG13150-0615-2S | CATHETER FG13150-0615-2S V04 | PhenomTM 21 Catheter | MICRO THERAPEUTICS, INC. | |
33 | 00847536041806 | FG13150-0615-2R | CATHETER FG13150-0615-2R V04 | PhenomTM 21 Catheter | MICRO THERAPEUTICS, INC. | |
34 | 00847536041790 | FG13150-0615-2J | CATHETER FG13150-0615-2J V04 | PhenomTM 21 Catheter | MICRO THERAPEUTICS, INC. | |
35 | 00847536041783 | FG11160-0615-2X | CATHETER FG11160-0615-2X V04 | PhenomTM 17 Catheter | MICRO THERAPEUTICS, INC. | |
36 | 00847536041776 | FG11160-0615-2S | CATHETER FG11160-0615-2S V04 | PhenomTM 17 Catheter | MICRO THERAPEUTICS, INC. | |
37 | 00847536041769 | FG11160-0615-2R | CATHETER FG11160-0615-2R V04 | PhenomTM 17 Catheter | MICRO THERAPEUTICS, INC. | |
38 | 00847536041752 | FG11160-0615-2J | CATHETER FG11160-0615-2J V04 | PhenomTM 17 Catheter | MICRO THERAPEUTICS, INC. | |
39 | 00847536041745 | FG11160-0615-1S | CATHETER FG11160-0615-1S V04 | PhenomTM 17 Catheter | MICRO THERAPEUTICS, INC. | |
40 | 00847536041738 | FG11150-0615-2X | CATHETER FG11150-0615-2X V04 | PhenomTM 17 Catheter | MICRO THERAPEUTICS, INC. | |
41 | 00847536041721 | FG11150-0615-2S | CATHETER FG11150-0615-2S V04 | PhenomTM 17 Catheter | MICRO THERAPEUTICS, INC. | |
42 | 00847536041714 | FG11150-0615-2R | CATHETER FG11150-0615-2R V04 | PhenomTM 17 Catheter | MICRO THERAPEUTICS, INC. | |
43 | 00847536041707 | FG11150-0615-2J | CATHETER FG11150-0615-2J V04 | PhenomTM 17 Catheter | MICRO THERAPEUTICS, INC. | |
44 | 00847536031784 | REACT-71 | CATHETER REACT-71 US V01 | ReactTM | MICRO THERAPEUTICS, INC. | |
45 | 00847536031777 | REACT-68 | CATHETER REACT-68 US V01 | ReactTM | MICRO THERAPEUTICS, INC. | |
46 | 00847536024625 | ARC-160 | CATHETER ARC-160 MINI V02 US CANADA | ArcTM | MICRO THERAPEUTICS, INC. | |
47 | 00847536024618 | ARC-132 | CATHETER ARC-132 V02 US CANADA | ArcTM | MICRO THERAPEUTICS, INC. | |
48 | 00847536021945 | MIC-021-150 | MICROCATHETER MIC-021-150 REVERSE | ReverseTM | REVERSE MEDICAL CORPORATION | |
49 | 00847536018044 | RFX072-95-08MP | RFX072-95-08MP DCS CATHETERS FG | NavienTM | MICRO THERAPEUTICS, INC. | |
50 | 00847536018020 | RFX072-95-08 | RFX072-95-08 DCS CATHETERS FG | NavienTM | MICRO THERAPEUTICS, INC. |