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Coronary stent Promus ELITE™
platinium-chromiumpolymerdrug eluting

Coronary stent - Promus ELITE™ - Boston Scientific - platinium-chromium / polymer / drug eluting
Coronary stent - Promus ELITE™ - Boston Scientific - platinium-chromium / polymer / drug eluting
Coronary stent - Promus ELITE™ - Boston Scientific - platinium-chromium / polymer / drug eluting - image - 2
Coronary stent - Promus ELITE™ - Boston Scientific - platinium-chromium / polymer / drug eluting - image - 3
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Characteristics

Type
coronary arteries
Material
platinium-chromium, polymer
Options
coated, drug eluting
Diameter

2.25 mm, 2.5 mm, 2.75 mm, 3 mm, 3.5 mm, 4 mm
(0.089 in, 0.098 in, 0.108 in, 0.118 in, 0.138 in, 0.157 in)

Length

8 mm, 12 mm, 16 mm, 20 mm, 24 mm, 28 mm, 32 mm, 38 mm
(0.315 in, 0.472 in, 0.63 in, 0.787 in, 0.945 in, 1.102 in, 1.26 in, 1.496 in)

Description

Summary
The Promus ELITE™ Stent System is a platinum‑chromium (PtCr) coronary stent system combining a customized stent architecture with Everolimus drug elution and a permanent PVDF‑HFP polymer coating. The device is engineered for optimized deliverability, radial strength and clinical performance, supported by extensive PLATINUM clinical data.

Product Details
The system integrates a PtCr stent platform, Everolimus drug with PVDF‑HFP permanent polymer, and an enhanced delivery catheter designed to balance pushability, flexibility and trackability for precise placement in coronary lesions.

Key features
  • Enhanced delivery system: optimized pushability, flexibility and trackability for improved lesion access.
  • Customized stent architecture: engineered to balance strength, conformability and scaffolding.
  • Drug and polymer: Everolimus combined with a permanent PVDF‑HFP polymer coating for controlled drug release.
  • Platform material: Platinum Chromium (PtCr) for radial strength and visibility.
  • Clinical evidence: extensive evaluation within the PLATINUM clinical trial program, including long‑term outcomes.


Ordering information (diameters, lengths and product codes)
(mm) | 8 | 12 | 16 | 20 | 24 | 28 | 32 | 38
2.25 | H7493941208220 | H7493941212220 | H7493941216220 | H7493941220220 | H7493941224220 | H7493941228220 | H7493941232220 | n/a
2.50 | H7493941208250 | H7493941212250 | H7493941216250 | H7493941220250 | H7493941224250 | H7493941228250 | H7493941232250 | H7493941238250
2.75 | H7493941208270 | H7493941212270 | H7493941216270 | H7493941220270 | H7493941224270 | H7493941228270 | H7493941232270 | H7493941238270
3.00 | H7493941208300 | H7493941212300 | H7493941216300 | H7493941220300 | H7493941224300 | H7493941228300 | H7493941232300 | H7493941238300
3.50 | H7493941208350 | H7493941212350 | H7493941216350 | H7493941220350 | H7493941224350 | H7493941228350 | H7493941232350 | H7493941238350
4.00 | H7493941208400 | H7493941212400 | H7493941216400 | H7493941220400 | H7493941224400 | H7493941228400 | H7493941232400 | H7493941238400

Clinical information
Nearly 10,000 patients have been evaluated across the PLATINUM clinical trial program, providing robust clinical evidence for safety and effectiveness across a wide patient population.

PLATINUM Workhorse Trial
  • Objective: Assess safety and effectiveness of the Promus PtCr Everolimus‑Eluting Coronary Stent System for patients with up to two de novo lesions ≤24 mm and vessel diameters ≥2.50 mm to ≤4.25 mm, versus Xience CoCr EES.
  • Design: Prospective, randomized, controlled, multicenter non‑inferiority trial.


Clinical outcomes
Five‑year results from the PLATINUM program report numerically lower event rates for the Promus ELITE™ Stent System within the PLATINUM family of studies.

Reimbursement
The C‑Code for the Promus ELITE™ Everolimus‑Eluting PtCr Coronary Stent System is C1874 (Stent, coated/covered with delivery system). C‑Codes are used for hospital outpatient device reporting for Medicare and some private payers; this is informational and not reimbursement or legal advice.

Key resources and documents
  • Product Brochure (Promus ELITE™)
  • Product Spec Sheet
  • Directions for Use
  • Indications, Safety and Warnings
  • Latex Information: Promus ELITE™
  • Metal Composition: Promus ELITE™
  • MRI Safety: Promus ELITE™


Technical specifications
  • Device name: Promus ELITE™ Everolimus‑Eluting Platinum Chromium Coronary Stent System
  • Drug: Everolimus
  • Polymer: PVDF‑HFP (permanent polymer)
  • Platform material: Platinum Chromium (PtCr)
  • Delivery system: enhanced for pushability, flexibility and trackability
  • Available diameters: 2.25 mm, 2.50 mm, 2.75 mm, 3.00 mm, 3.50 mm, 4.00 mm
  • Available lengths (mm): 8, 12, 16, 20, 24, 28, 32, 38 (availability varies by diameter; see ordering codes above)
  • Clinical evidence: Extensive PLATINUM clinical trial program including PLATINUM Workhorse and related studies
  • Regulatory/usage note: CAUTION — restricted to sale by or on the order of a physician; follow product labeling for indications, contraindications, warnings and instructions for use.
*Prices are pre-tax. They exclude delivery charges and customs duties and do not include additional charges for installation or activation options. Prices are indicative only and may vary by country, with changes to the cost of raw materials and exchange rates.