Company Name	Product Name	Drug Type	Drug Concentration (µg/mm2)	Excipient Type	Guidewire Compatibility (inch)	Shaft Length (cm)	Sheath Compatibility (F)	Balloon Diameters (mm)	Balloon Lengths (cm)
BD Interventional	Lutonix 035 Drug Coated Balloon PTA Catheter	Paclitaxel	2	Polysorbate and sorbitol	0.035	75, 100, 130	5, 7, 8, 10	4, 5, 6, 7, 8, 9, 10, 12	4, 6, 8, 10, 12, 15
BD Interventional	Lutonix 018 Drug Coated Balloon PTA Catheter	Paclitaxel	2	Polysorbate and sorbitol	0.018	100, 130	4, 5	4, 5, 6, 7	4, 6, 8, 10, 12, 15, 22
BD Interventional	Lutonix 014 Drug Coated Balloon PTA Catheter	Paclitaxel	2	Polysorbate and sorbitol	0.014	150	4	2, 2.5, 3, 3.5, 4	4, 8, 12, 15

Company Name	Product Name	Nominal Pressure (atm)	Rated Burst Pressure (atm)	Guidewire Compatibility (inch)	Shaft Length (cm)	Sheath Compatibility (F)	Balloon Diameters (mm)	Balloon Lengths (cm)
BD Interventional	Dorado 40 PTA Dilatation Catheter	8	20–24	0.035	40, 80, 120, 135	5, 6, 7	3, 4, 5, 6, 7, 8, 9, 10	2, 4, 6, 8, 10, 12, 15, 17, 20
BD Interventional	Atlas Gold PTA Dilatation Catheter	4–6	12–18	0.035	80, 120	7, 8, 9, 10, 12	12, 14, 16, 18, 20, 22, 24, 26	2, 4, 6
BD Interventional	Conquest 40 PTA Dilatation Catheter	8	30–40	0.035	50, 75	6, 7, 8	4, 5, 6, 7, 8, 9, 10, 12	2, 3, 4, 6, 8, 10
BD Interventional	Conquest PTA Dilatation Catheter	8	20–30	0.035	50, 75, 120	6, 7, 8	5, 6, 7, 8, 9, 10, 12	2, 3, 4, 6, 8
BD Interventional	LitePAC Rapid Exchange PTA Balloon Catheter	6	12–16	0.014	150, 155	4, 5	2, 2.5, 3, 3.5, 4, 5, 5.5, 6, 7	1.5, 2, 3, 4, 5, 6, 8, 10, 12, 15, 18, 20, 22
BD Interventional	Ultraverse 014 PTA Dilatation Catheter	6	13–16	0.014	150	4, 5	1.5, 2, 3, 3.5, 4, 5	2, 4, 8, 10, 12, 15, 22, 30
BD Interventional	Ultraverse 018 PTA Dilatation Catheter	6	11–16	0.018	75, 130, 200	4, 5, 6	2, 2.5, 3, 3.5, 4, 5, 6, 7, 8, 9	2, 4, 6, 8, 10, 12, 15, 20, 22, 30
BD Interventional	Ultraverse 035 PTA Balloon Dilatation Catheter	6–8	9–21 (depending on size)	0.035	75, 130	5, 6, 7	3, 4, 5, 6, 7, 8, 9, 10, 12	2, 4, 6, 8, 10 , 12, 15, 20, 25, 30
BD Interventional	Ultraverse RX PTA Dilatation Catheter	6	12–16	0.014	150, 200	4, 5	1.25, 1.5, 2, 2.5, 3, 3.5, 4, 5, 6, 7	1.5, 2, 4, 8, 10, 12, 15,20, 30

Company Name	Product Name	Nominal Pressure (atm)	Rated Burst Pressure (atm)	Guidewire Compatibility (inch)	Size (F)	Sheath Compatibility (F)	Shaft Length (cm)	Balloon Diameters (mm)	Balloon Lengths (cm)
BD Interventional	UltraScore Focused Force PTA Balloon	6–8	Up to 14	0.014 (2–7 mm), 0.035 (4–8 mm)	–	4, 5, 6	130, 150	2, 2.5, 3, 3.5, 4, 5, 6, 7, 8, 9, 10, 12	2, 4, 8, 10, 12, 15, 20, 30
BD Interventional	True Flow Valvuloplasty Perfusion Catheter	3	6	0.035	–	11, 12, 14, 16	110	18, 20, 22, 24, 26	3.5
BD Interventional	True Dilatation Balloon Valvuloplasty Catheter	3	6	0.035	–	11–14	110	18–28	4.5

Company Name	Product Name	Catheter Size (F)	Working Length (cm)	Minimum Guiding Catheter ID (inch)	Comments
BD Interventional	Seeker Crossing Support Catheters	4 (0.014-inch wire, 0.018-inch wire), 5 (0.035-inch wire)	65, 90, 135, 150	4, 5 F	Hydrophilic-coated support catheter with a 30-cm radiopaque marking system (1 cm in length, positioned 1 cm apart), sized to support standard 0.014-, 0.018-, and 0.035-inch guidewires

Company Name	Product Name	Size (F)	Length (cm)	Guidewire Compatibility (inch)	Curved or Straight	Radiopaque Tip	Hydrophilic Coating
BD Interventional	Halo One Thin-Walled Guiding Sheath	4, 5, 6	10, 25, 45, 70, 90	0.018, 0.035	Straight	Yes	Yes

Company Name	Product Name	Material Used	Maximum Guidewire Size (inch)	Introducer Size (F)	Stent Diameter (mm)	Stent Length (mm)	Delivery System Length (cm)	CE Mark Indications
BD Interventional	LifeStream Balloon-Expandable Vascular Covered Stent	316L stainless steel and ePTFE	0.035	6, 7, 8	5, 6, 7, 8, 9, 10, 12	16, 26, 37, 38, 58	80, 135	Indicated for the treatment of atherosclerotic lesions in common and external iliac arteries

Company Name	Product Name	Material Used	Introducer Size (F)	Guidewire Compatibility (inch)	Stent Diameter (mm)	Stent Length (mm)	Delivery System Length (cm)	CE Mark Indications
BD Interventional	LifeStent Solo Vascular Stent System	Nitinol	6	0.035	6, 7	200	80, 135	Intended to improve luminal diameter in the treatment of symptomatic de novo or restenotic lesions in the native superficial femoral artery and proximal popliteal artery
BD Interventional	E-Luminexx Biliary Stent	Nitinol	6	0.035	8, 10	40, 60, 80, 100	60	Treatment of biliary strictures resulting from malignant neoplasms
BD Interventional	E-Luminexx Vascular Stent	Nitinol	6	0.035	6, 7, 8, 9, 10, 12, 14	20, 30, 40, 50, 60, 80, 100, 120	80, 135	Residual stenosis with impaired perfusion (pressure gradient) following balloon dilatation, especially in stages III and IV according to Fontaine; dissection; detached arteriosclerotic plaque material and luminal obstruction following balloon dilatation; occlusion after thrombolysis or after aspiration and before dilatation; restenosis or reocclusion
BD Interventional	LifeStar Vascular Stent System	Nitinol	6	0.035	6, 7, 8, 9, 10, 12, 14	20, 30, 40, 50, 60, 80, 100, 120	80, 135	Residual stenosis with impaired perfusion (pressure gradient) following balloon dilatation, especially in stages III and IV according to Fontaine; dissection; detached arteriosclerotic plaque material and luminal obstruction following balloon dilatation; occlusion after thrombolysis or after aspiration and before dilatation; restenosis or reocclusion
BD Interventional	LifeStent 5F Vascular Stent System	Nitinol	5	0.035	5, 6, 7	20, 30, 40, 60, 80, 100, 120, 150, 170 (diameter dependent)	80, 135	Intended to improve luminal diameter in the treatment of symptomatic de novo or restenotic lesions in the native superficial femoral artery and popliteal artery
BD Interventional	LifeStent Vascular Stent System	Nitinol	6	0.035	8, 9, 10, 12, 14	20, 30, 40, 60, 80 (diameter dependent)	80, 130	Intended for primary stenting of de novo or restenotic lesions of the peripheral arteries (20–170 mm); primary stenting of the SFA and/or the PPA (200 mm)
BD Interventional	LifeStent XL Vascular Stent System	Nitinol	6	0.035	6, 7	200	80, 135	Intended for primary stenting of de novo or restenotic lesions of the peripheral arteries (20–170 mm); primary stenting of the SFA and/or the PPA (200 mm)

Company Name	Product Name	Materials Used	Introducer Size (F)	Guidewire Compatibility (inch)	Stent Diameter (mm)	Stent Length (mm)	Delivery System Length (cm)	CE Mark Indications	Comments
BD Interventional	Fluency Plus Endovascular Stent Graft	Nitinol/ePTFE	8, 9, 10	0.035	5, 6, 7, 8, 9, 10, 12, 13.5	20, 30, 40, 60, 80, 100, 120	80, 117	Residual stenosis with impaired perfusion (pressure gradient) after balloon dilatation, especially in stages III and IV according to Fontaine; dissection; detached arteriosclerotic plaque material and luminal obstruction after balloon dilatation; occlusion after thrombolysis or after aspiration and before dilatation; restenosis or reocclusion	–
BD Interventional	Covera Plus Vascular Covered Stent	Nitinol	8, 9	0.035	6, 7, 8, 9, 10	30, 40, 60, 80, 100	80, 120	Indicated for the treatment of stenoses in the upper extremity venous outflow of patients dialyzing with an AV access graft or fistula and for the treatment of atherosclerotic lesions in iliac and femoral arteries with a reference vessel diameter of 4.5–9 mm	–
BD Interventional	Covera Vascular Covered Stent	Nitinol, ePTFE-covered stent	8, 9	0.035	6, 7, 8, 9,10	30, 40, 60, 80, 100	80, 120	Indicated for use in hemodialysis patients for the treatment of stenoses in the venous outflow of an arterio-venous (AV) fistula and at the venous anastomosis of an ePTFE or other synthetic AV graft	–

Company Name	Product Name	Stent Material	Cell Design	Introducer Size (F)	Guidewire Compatibility (inch)	Stent Diameter (mm)	Stent Length (mm)	Delivery System	Delivery System Length (cm)
BD Interventional	Venovo Venous Stent System	Nitinol	Open-cell	8, 9, 10	0.035	10, 12, 14, 16, 18, 20	40, 60, 80, 100, 120, 140, 160	Triaxial, thumbwheel	80, 120

Company Name	Product Name	Minimum Vessel Diameter (mm)	Sheath Compatibility (F)	Crossing Profile (inch)	Working Length (cm)	Tip Length (cm)
BD Interventional	RotarexS Rotational Atherothrombectomy System	3	6	0.079 (2 mm)	110, 135	–
BD Interventional	RotarexS Rotational Atherothrombectomy System	7	10	0.131 (3.33 mm)	85	–
BD Interventional	RotarexS Rotational Atherothrombectomy System	5	8	0.105 (2.67 mm)	85, 110	–

Company Name	Product Name	Size (F)	Tip-to-Cuff Insertion Length (cm)	Tip Type	Number of Lumens	Sideholes (Yes/No)	Coated (Yes/No)	Acute or Chronic
BD Interventional	EquiStream Long-Term Hemodialysis Catheter	14.5	15, 19, 23, 27, 31, 35, 42 (straight); 19, 24, 28, 31 (AlphaCurve)	Split tip	Two	Yes	No	Chronic
BD Interventional	EquiStream XK Long-Term Hemodialysis Catheter	16	19, 23, 27, 31, 35, 42 (straight); 19, 24, 28, 31 (alphacurve)	Split tip	Two	Yes	No	Chronic
BD Interventional	GlidePath Long-Term Dialysis Catheter	14.5	15, 19, 23, 27, 31, 35, 42, (straight); 19, 24, 28, 31 (alphacurve)	Symmetric	Dual	Yes	No	Chronic
BD Interventional	HemoSplit Long-Term Hemodialysis Catheter	14.5	15, 19, 23, 27, 31, 35, 42 (straight); 19, 24, 28, 31 (AlphaCurve)	Split tip	Two	Yes	No	Chronic
BD Interventional	HemoSplit XK Long-Term Hemodialysis Catheter	16	19, 23, 27, 31, 35, 42 (straight); 19, 24, 28, (alphacurve)	Split tip	Two	Yes	No	Chronic
BD Interventional	HemoStar Long-Term Hemodialysis Catheter	14.5	15, 19, 23, 27, 31, 35, 42 (straight); 19, 24, 28, 31 (AlphaCurve)	Staggered	Two	Yes	No	Chronic
BD Interventional	HemoStar XK Long-Term Hemodialysis Catheter	16	19, 23, 27, 31, 35, 42 (straight); 19, 24, 28, (alphacurve)	Staggered	Two	Yes	No	Chronic

Company Name	Product Name	Technology	Wavelength (nm)	Sheath Size (F)	Sheath Length (cm)	CE Mark Indications
BD Interventional	Venclose RF Ablation System	Radiofrequency	Adjustable heating length (2.5 cm/10 cm)	6 (with working length of 60 cm and 100 cm)	7, 12	Intended for endovascular coagulation of blood vessels in patients with superficial vein reflux
BD Interventional	Venclose Radiofrequency Generator	Radiofrequency	–	–	–	Intended for endovascular coagulation of blood vessels in patients with superficial vein reflux

Company Name	Product Name	Materials Used	Nitinol Reinforced Section Diameter (mm)	Nitinol Reinforced Section Length (cm)	Vascular Graft Section Introducer Size (F)	Vascular Graft Section Recommended Guidewire (inch)	Introducer Size (F)	Recommended Guidewire (inch)	CE Mark Indications
BD Interventional	Carboflo Vascular Graft	ePTFE with carbon impregnated into the inner portions of the graft wall	4, 5, 6, 7, 8, 10	1, 2, 3, 4, 5, 6, 7, 8	–	–	–	–	Indicated for use as vascular prostheses
BD Interventional	Distaflo Bypass Graft	ePTFE with carbon impregnated into the inner portions of the graft wall; graft is also modified with a proprietary cuff at the distal end	6, 7, 8	50, 60, 70, 80	–	–	–	–	Intended for bypass or reconstruction of peripheral arterial blood vessels
BD Interventional	Venaflo II Vascular Graft	Vascular ePTFE grafts for haemodialysis	4-7	1, 2 , 2.5, 3, 3.5, 4, 4.5, 5	–	–	–	–	–

Company Name	Product Name	Sheath Compatibility (F)	Guidewire Compatibility (inch)	Working Length (cm)	Mode of Operation	CE Mark Indications
BD Interventional	AspirexS: Mechanical Aspiration Thrombectomy System	8	0.018	85, 110	Aspirex S catheters in combination with the Straub Medical Drive System (REF SRS-Set/80300) are intended for the percutaneous transluminal removal of fresh thrombotic or thromboembolic material from blood vessels outside the cardiopulmonary, coronary, and cerebral circulations	Native blood vessels or vessels fitted with stents, stent grafts, or native or artificial bypasses outside the cardiopulmonary, coronary, and cerebral circulations
BD Interventional	AspirexS: Mechanical Aspiration Thrombectomy System	10	0.025	110	Aspirex S catheters in combination with the Straub Medical Drive System (REF SRS-Set/80300) are intended for the percutaneous transluminal removal of fresh thrombotic or thromboembolic material from blood vessels outside the cardiopulmonary, coronary, and cerebral circulations	Native blood vessels or vessels fitted with stents, stent grafts, or native or artificial bypasses outside the cardiopulmonary, coronary, and cerebral circulations
BD Interventional	AspirexS: Mechanical Aspiration Thrombectomy System	6	0.018	110, 135	Aspirex S catheters in combination with the Straub Medical Drive System (REF SRS-Set/80300) are intended for the percutaneous transluminal removal of fresh thrombotic or thromboembolic material from blood vessels outside the cardiopulmonary, coronary, and cerebral circulations	Native blood vessels or vessels fitted with stents, stent grafts, or native or artificial bypasses outside the cardiopulmonary, coronary, and cerebral circulations
BD Interventional	RotarexS Rotational Atherothrombectomy System	8	0.018	85, 110	RotarexS catheters in combination with the Straub Medical Drive System (REF SRS-Set/80300) are intended for the percutaneous transluminal removal of thrombotic, thromboembolic and atherothrombotic material from fresh, subacute and chronic occlusions of blood vessels outside the cardiopulmonary, coronary and cerebral circulations	Native blood vessels or vessels fitted with stents, stent grafts or native or artificial bypasses outside the cardiopulmonary, coronary and cerebral circulations
BD Interventional	RotarexS Rotational Atherothrombectomy System	10	0.025	85	RotarexS catheters in combination with the Straub Medical Drive System (REF SRS-Set/80300) are intended for the percutaneous transluminal removal of thrombotic, thromboembolic and atherothrombotic material from fresh, subacute and chronic occlusions of blood vessels outside the cardiopulmonary, coronary and cerebral circulations	Native blood vessels or vessels fitted with stents, stent grafts or native or artificial bypasses outside the cardiopulmonary, coronary and cerebral circulations
BD Interventional	RotarexS Rotational Atherothrombectomy System	6	0.018	110, 135	RotarexS catheters in combination with the Straub Medical Drive System (REF SRS-Set/80300) are intended for the percutaneous transluminal removal of thrombotic, thromboembolic and atherothrombotic material from fresh, subacute and chronic occlusions of blood vessels outside the cardiopulmonary, coronary and cerebral circulations	Native blood vessels or vessels fitted with stents, stent grafts or native or artificial bypasses outside the cardiopulmonary, coronary and cerebral circulations

Company Name	Product Name	Size (F)	Maximum Guidewire Compatibility (inch)	Catheter Working Length (cm)	Recommended Introducer Size (F)	Fistula Site(s)	Outflow	Access	Mechanism of Action	AV Connection	Energy Source	Imaging Guidance	Adjunctive Procedures
BD Interventional	WavelinQ EndoAVF System	4	0.014	43 (venous catheter); 50 (arterial catheter)	5	(1) Concomitant ulnar artery and ulnar vein; or (2) concomitant radial artery and radial vein	Split-flow fistula (cephalic or basilic vein)	Venous and arterial	Radiofrequency ablation	Platelet deposition and endothelium development of fistula tract	Electrosurgical unit (BD ESU-1)	Fluoroscopy and ultrasound	Recommended embolization of a brachial vein at index procedure

Company Name	Product Name	Catheter Size/Length (F/cm)	Working Diameters (mm)	Snare Length (cm)	Snare Type
BD Interventional	Bard Snare Retrieval Kit	6/9/11	20	58	Convenient all-in-one, easy-to-use kit; the snare catheter and helical loop are provided together with the dual sheath and the dilator

Company Name	Product Name	Indicated Caval Diameter (mm) (based on average caval diameter)	Maximum Deployed Length (mm)	Catheter Carrier System ID (F)	Material	Design	Approach	Permanent/Retrievable
BD Interventional	Denali Vena Cava Filter	Up to 28	51	8.4	Nitinol	Conical, two-level filtration	Femoral/jugular	Optional (permanent or retrievable)

Company Name	Product Name	Color	Pressure Range (atm)	Barrel Volume (mL)	Luminescent Gauge (Yes/No)	Gauge	Latch Type	Threads
BD Interventional	Presto Inflation Device	Blue/white	0–40	30	No	Angled	–	–