
AGENT Paclitaxel-Coated PTCA Balloon Catheter 2 X 12 | REF H74939222201210
Boston Scientific AGENT Paclitaxel-Coated PTCA Balloon Catheter, 2.0 mm x 12 mm (REF H74939222201210) — drug-coated balloon for coronary intervention.

The Cordis NEON NC Non-Compliant PTCA Balloon Catheter (REF BN20020, 2.0 mm x 20 mm) is a rapid-exchange coronary balloon engineered for predictable high-pressure performance during percutaneous transluminal coronary angioplasty (PTCA) and stent post-dilatation procedures. Its non-compliant balloon material is intended to maintain consistent diameter under high inflation pressures, supporting controlled lesion preparation and stent apposition.
Key Features
- Non-compliant balloon technology for minimal diameter growth at high pressures
- Balloon dimensions: 2.0 mm diameter x 20 mm length
- Rapid-exchange (monorail) catheter design for single-operator use
- Low-profile tip intended to facilitate crossing of tight or calcified lesions
- Hydrophilic-style shaft coating to support trackability and pushability
- Radiopaque marker bands for fluoroscopic balloon positioning
- Compatible with standard 0.014" coronary guidewires
- Rated burst and nominal pressures: Not specified in the located sources
Clinical Applications
- Post-dilatation and optimization of deployed coronary stents
- High-pressure dilatation of resistant or fibrocalcific coronary lesions
- Treatment of in-stent restenosis as part of a PCI strategy
- Adjunctive lesion preparation in complex coronary anatomy
Product Information
Brand: Cordis
Product Family: NEON NC Non-Compliant PTCA Balloon
Category: Coronary Balloon Catheters
REF / UPN: BN20020
Balloon Diameter: 2.0 mm
Balloon Length: 20 mm
Catheter Type: Rapid-exchange PTCA balloon catheter
Guidewire Compatibility: 0.014" coronary guidewire
Guide Catheter Compatibility: Not specified in the located sources
Usable Catheter Length: Not specified in the located sources
Sterilization: Supplied sterile, single-use device
Regulatory Status: Refer to the manufacturer Instructions for Use (IFU) for market-specific approvals and indications.
Tell us what product you need and share a few details.
We connect your request with the most relevant verified brands.
Relevant supplier options can respond with availability, documentation context, and quote details.
Practical answers for procurement teams reviewing this product page.
Include the exact product family, brand preference, REF/UPN code when available, required quantity, destination country, expected delivery timing and documentation expectations.
Yes. If alternatives are acceptable, mention equivalent brands, compatible models, size ranges and any non-negotiable requirements.
Related products are connected through structured catalog data such as brand, category, product family and country assignment.
No. This page supports sourcing and RFQ organization. Buyers must verify regulatory status, clinical suitability and procurement compliance independently.
Specific codes reduce ambiguity and help supplier teams identify product availability, packaging details and documentation faster.
Yes. The workflow is designed for hospitals, clinics, distributors, wholesalers, importers and procurement departments.
Yes. Products can be connected to multiple countries in the admin panel, and buyers can specify destination details in the RFQ form.
The request is stored with contact and procurement details so the sourcing conversation can be reviewed and followed up clearly.