B Braun Interventional Systems, Inc
14 product lines across 9 device categories: Angioplasty balloons, Biliary drains, Angiographic catheters, Guidewires, Implanted ports, IVC filters.
From bisusa.com, checked October 2026.
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About B Braun Interventional Systems, Inc
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Peripheral Angioplasty Balloons
Used in: DVT Mechanical Thrombectomy, Venous Stenting (Iliac and Central Veins), Peripheral Balloon Angioplasty, Peripheral Artery Stenting, Peripheral Atherectomy, Fistulogram with Angioplasty
Biliary Drainage Catheters
Used in: Percutaneous Biliary Drainage (PTBD)
| Product | Sizes (FDA GUDID) | Models | MRI |
|---|---|---|---|
| Accel ACCEL APD 14F 25CM W/ LOCK | Length: 15–40 cm | 38 | Not stated |
Angiographic Catheters
Used in: Uterine Artery Embolization (UAE), Internal Iliac Artery Embolization
| Product | Sizes (FDA GUDID) | Models | MRI |
|---|---|---|---|
| Multi-Track MULTITRACK ANGIO CATH 3.0F,80" | Length: 100 cm | 10 | Not stated |
Guidewires
Used in: Uterine Artery Embolization (UAE), Peripheral Balloon Angioplasty, Stroke Thrombectomy, Internal Iliac Artery Embolization
Implanted Ports (Port-a-Cath)
IVC Filters
Used in: IVC Filter Placement
| Product | Sizes (FDA GUDID) | Models | MRI |
|---|---|---|---|
| Vena Tech VenaTech® LP Brachial Introducer System | Catheter Gauge: 9–12.9 Fr | 3 | Not stated |
Nephrostomy and Nephroureteral Catheters
Used in: Nephrostomy Tube Placement, Nephroureteral Stent (PCNU) Placement
| Product | Sizes (FDA GUDID) | Models | MRI |
|---|---|---|---|
| Accel ACCEL APD 14F 25CM W/ LOCK | Length: 15–40 cm | 38 | Not stated |
PICC Lines and Midline Catheters
Used in: PICC Line Placement
| Product | Sizes (FDA GUDID) | Models | MRI |
|---|---|---|---|
| B.braun 6F PICC DUAL 60 NITGOLD 80 CTD660-NG80 | Catheter Gauge: 4–6 Fr | 10 | Not stated |
Tunneled Pleural and Peritoneal Catheters (PleurX)
Used in: Tunneled Peritoneal Catheter (PleurX) Placement, Tunneled Pleural Catheter Placement
| Product | Sizes (FDA GUDID) | Models | MRI |
|---|---|---|---|
| Asept ASEPT PERITONEAL DRAINAGE SYSTEM | — | 1 | Not stated |
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From bisusa.com, checked October 2026.
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FDA clearances and approvals
- venatech convertible vena cava filter system 510K K152765, 2016
Product lines, models and sizes are compiled from the FDA Global Unique Device Identification Database (GUDID) and FDA clearance records. Descriptions marked "Provided by the manufacturer" come from the company and are reviewed before publishing.