Pioneering the Future of Large-Bore Vessel Closure for Arterial and Venous Access

PerQseal Elite - Pioneering the Future of Large-Bore Vessel Closure for Arterial and Venous Access

PerQseal®Elite is CE Mark approved. Not available for sale in the United States.

PerQseal®Elite Setting a new standard in procedural efficiency and patient care.

Our flagship PerQseal® technology is the first of its kind: a 100% bio-absorbable, sutureless patch-based large-bore closure system designed specifically for Arterial and Venous Access. Engineered for simplicity, safety, and performance, PerQseal eliminates the need for sutures, collagen, or metal, it supports healing, leaving nothing behind and restoring the vessel to its natural state within 180 days3.

Downloads

PerQseal Elite Brochure

Click to download PDF brochure

Device Performance & Improved Patient Benefit

97% Technical success (Per-protocol population)
0% Major device related complications (VARC-3 Definitions)

Data on file at Vivasure Medical – Elite Arterial Study P935-00

Seals and Heals from Inside

The external fixation enhances the compression of the implant to seal the access site from within the vessel with precision and control, minimizing trauma and potentially reducing risk of complications.

Seals and Heals from Inside

Unique Patch Design Utilizes Body’s Healing Mechanism4

Using advanced polymer technology, PerQseal Elite seals the access site with a 100% bio-absorbable implant made from Polydioxanone (PDO) that fully biodegrades within 180 days, restoring the vessel to its natural state3.

Unique Patch Design Utilizes Body’s Healing Mechanism

3&4  Pre-clinical data on file at Vivasure Medical
5. Patch explanted at 24 hours

Sutureless & 100% bio-absorbable

Leave nothing behind! No sutures, collagen, or metal implants, just a fully synthetic patch that naturally degrades over time.3

Sutureless & 100% bio-absorbable

Indication for use

The PerQseal® Elite Single-use device is indicated for the percutaneous sealing of a common femoral arteriotomies/venotomies in patients following interventional therapeutic endovascular procedures created with sheath sizes 14 – 22 F (arteriotomy/venotomy up to 26 F).

Ordering Information

 

Catalogue Number

Contents

DP4-P1-2-G

PerQseal Elite Closure Device + PerQseal Elite Introducer Sheath

The PerQseal ELITE Closure Device and PerQseal ELITE Introducer are CE mark approved.
To check the Eudamed database for information on the PerQseal ELITE device please use the following reference.
Basic UDI-DI: 539153318DP4FA1VCDV7 https://ec.europa.eu/tools/eudamed (when available)