The Boston Scientific AcoArt Drug-Coated Balloon (REF LTS20120DG) is a single-use peripheral balloon dilatation catheter featuring a paclitaxel drug coating intended to support local antiproliferative drug transfer to the vessel wall during percutaneous transluminal angioplasty. With a labeled balloon diameter of 2.0 mm and a working length of 120 mm, this device is configured for treatment of long, narrow peripheral vessel segments where uniform drug delivery and predictable balloon compliance are operationally important.
Key Features
- Paclitaxel-based drug coating engineered for controlled transfer to the target vessel wall
- Balloon diameter: 2.0 mm
- Balloon working length: 120 mm
- Over-the-wire compatible peripheral balloon platform
- Low-profile design intended to facilitate crossing of tight, tortuous lesions
- Single-use, sterile, supplied in protective packaging
- Catalog markings reference 4 and 17 per the original product label; refer to the manufacturer IFU for full sizing matrix and shaft length confirmation
Clinical Applications
- Percutaneous transluminal angioplasty of peripheral arteries
- Treatment of below-the-knee and small-caliber peripheral lesions where a 2.0 mm working diameter is appropriate
- Long-segment lesion treatment supported by the 120 mm balloon length
- Adjunctive use within peripheral revascularization workflows as defined by the official Instructions for Use
- Procedure suitability, patient selection and contraindications must follow the manufacturer IFU and applicable local regulatory labeling
Product Information
- Brand: Boston Scientific
- Product line: AcoArt Drug-Coated Balloon 150
- Category: Peripheral Balloon Catheters
- REF / UPN: LTS20120DG
- Balloon diameter: 2.0 mm
- Balloon length: 120 mm
- Drug coating: Paclitaxel-based (refer to IFU for dose density)
- Catheter shaft length: Not specified in the located sources
- Guidewire compatibility: Not specified in the located sources
- Rated burst pressure / nominal pressure: Not specified in the located sources
- Sterility: Sterile, single-use
- Regulatory status, approved indications and market availability vary by region; verify against current manufacturer documentation before procurement