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ACURATE Prime™ Aortic Valve System


Prime Performance.
Today and Tomorrow.​

A Self-Expanding Valve Designed for TAVI Precision.

ACURATE Prime™ is a self-expanding, supra-annular valve designed to optimise outcomes in transcatheter aortic valve implantation (TAVI) procedures. With proven ease of use, predictable performance, while preserving future coronary access, it supports precision at every step of TAVI.​


Acurate Prime TiltedOpen

Introducing the ACURATE Prime™ Aortic Valve System

Designed to support precision during every TAVI procedure, ACURATE Prime features a split-level design, top-down deployment, and predictable commissural alignment.​

​Whether for a first-time TAVI procedure or a complex TAVI-in-TAVI case, its open-cell frame design and supra-annular leaflets provide consistent hemodynamic performance and post-procedure access flexibility.​​

Elevate your TAVI experience with ACURATE Prime. ​

  • Expanded treatment range​
  • Enhanced valve frame​
  • Quicker, controlled deployment​
  • Streamlined device preparation​

ACURATE Prime Evolves​

Expanded Treatment Range

ACURATE Prime™ has a broad size matrix to accommodate a wide range of annulus diameters, enabling treatment in both standard and complex TAVI procedures.​

Valve size23 mm25 mm27 mm29 mm
Aortic annulus diameter*20.5 mm - 23 mm22.5 mm - 25 mm24.5 mm - 27 mm26.5 mm - 29 mm
Aortic annulus perimeter64 mm - 72 mm71 mm - 79 mm77 mm - 85 mm83 mm - 91 mm

Connected Cell

ACURATE neo and ACURATE prime

Built to enhance control and efficiency, ACURATE Prime™ delivers reliable performance in a variety of TAVI procedures.​

45% Faster loading time compared to ACURATE neo2TM 1​

24% Fewer loading components compared to ACURATE neo2TM 1​

90° Controlled Instant ​Release

More Precise Positioning Marker​


Why ACURATE Prime​

Implant with Ease

  • Streamlined device preparation and smooth deliverability
  • Quicker deployment and predictable commissure alignment¹
  • Precise and consistent positioning²

Maximise Outcomes

  • Low PPI rates³
  • Single-digit gradients³
  • Excellent PVL rates²

Optimise Lifetime Patient Management

  • Unrestricted coronary access⁴
  • Maintained stable hemodynamic function³
  • Engineered to last⁵

Early ACURATE Prime Registry

The Early ACURATE Prime Registry is the first real-world study evaluating the ACURATE PrimeTM Aortic Valve System.​

​This prospective, multicenter registry enrolled N=517 patients to assess the 30-day performance of the ACURATE Prime Aortic Valve System. The results demonstrated an excellent safety and efficacy profile in a real-world clinical setting.​

Below are the key 30-day outcomes as presented by Dr. Andreas Rück at EuroPCR 2025:​

  • ​98.6% Technical Success​​
  • 1.2% ≥ Moderate PVL​s​
  • 7.2 mmHg Mean Gradients​​
  • 9.8% New Pacemakers​​​
  • 0.4% 30-days Mortality

EarlyPrime EuroPCR 2025 - Conference Presentation

Early ACURATE Prime Registry:
30 day results

Filename
SH-2209704 AA-EarlyPrime-EuroPCR-2025-Conference-Presentation-Slides.pdf
Size
1 MB
Format
application/pdf
View the presentation


*CT-based measurement: Perimeter-derived annulus.

1. Bieliauskas G, Wong I, Bajoras V, et al. Patient-Specific Implantation Technique to Obtain Neo-Commissural Alignment With Self-Expanding Transcatheter Aortic Valves. JACC Cardiovasc Interv. 2021 October 11;14(19):2097–2108.
​2. Kim WK, Tamburino C, Möllmann H, et al. Clinical outcomes of the ACURATE neo2 transcatheter heart valve: a prospective, multicenter, observational, post-market surveillance study. EuroIntervention. 2023;19(1):83-92​
3. Rück A, Kim WK, Abdel-Wahab M, et al. The Early neo2 Registry: Transcatheter Aortic Valve Implantation with ACURATE neo2 in a European Population. J Am Heart Assoc. 2023 Aug;12(15):e029464
4. Barbanti M, Costa G, Picci A, et al. Coronary Cannulation After Transcatheter Aortic Valve Replacement: The RE-ACCESS Study. JACC Cardiovasc Interv. 2020 Nov 9;13(21):2542-2555.
5. Möllmann et al. Five-year outcomes of transcatheter aortic valve implantation with the ACURATE neo2 valve system, EuroIntervention 2024, e951-e953, 10.4244/EIJ-D-23-00852

CAUTION: The law restricts these devices to sale by or on the order of a physician. Indications, contraindications, warnings, and instructions for use can be found in the product labelling supplied with each device or at www.IFU-BSCI.com. Products shown for INFORMATION purposes only and may not be approved or for sale in certain countries. This material not intended for use in France. 2024 Copyright © Boston Scientific Corporation or its affiliates. All rights reserved.

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