The Tack Endovascular System is a first-of-its-kind, minimal-metal dissection repair device, purpose-built for precision treatment of post-PTA peripheral arterial dissections to promote healing, improve outcomes, and preserve limbs.¹
Door op de link te klikken, verlaat u de officiële website van Royal Philips Healthcare ("Philips"). Alle links naar websites van derden die op deze site kunnen verschijnen, zijn alleen bedoeld voor uw gemak en vertegenwoordigen op geen enkele manier enige aansluiting bij of goedkeuring van de informatie die op die gelinkte websites wordt verstrekt. Philips geeft geen verklaringen of garanties van welke aard dan ook met betrekking tot websites van derden of de daarin opgenomen informatie.
You are about to visit a Philips global content page
You are about to visit the Philips USA website.
Media galerij
Kenmerken
Purpose built
Purpose built
The Tack endovascular system is purpose-built to repair peripheral arterial dissections following balloon angioplasty in ATK and BTK therapeutic interventions.
Purpose built
The Tack endovascular system is purpose-built to repair peripheral arterial dissections following balloon angioplasty in ATK and BTK therapeutic interventions.
Purpose built
The Tack endovascular system is purpose-built to repair peripheral arterial dissections following balloon angioplasty in ATK and BTK therapeutic interventions.
The Tack endovascular system is purpose-built to repair peripheral arterial dissections following balloon angioplasty in ATK and BTK therapeutic interventions.
Precision repair
Precision repair
Focal treatment with minimal metal treats only the area where dissections are present and avoids covering portions of healthy tissue.
Precision repair
Focal treatment with minimal metal treats only the area where dissections are present and avoids covering portions of healthy tissue.
Precision repair
Focal treatment with minimal metal treats only the area where dissections are present and avoids covering portions of healthy tissue.
Leaves behind significantly less metal than stents, preserving vessel integrity, future treatment options and—ultimately—limbs.
Adaptive sizing
Adaptive sizing
Only the Tack endovascular system features adaptive sizing – which allows each Tack implant to adapt to tapering anatomy while maintaining a relatively constant radial force. This means that a single size Tack implant can be used across a wide range of vessel diameters.
Adaptive sizing
Only the Tack endovascular system features adaptive sizing – which allows each Tack implant to adapt to tapering anatomy while maintaining a relatively constant radial force. This means that a single size Tack implant can be used across a wide range of vessel diameters.
Adaptive sizing
Only the Tack endovascular system features adaptive sizing – which allows each Tack implant to adapt to tapering anatomy while maintaining a relatively constant radial force. This means that a single size Tack implant can be used across a wide range of vessel diameters.
Only the Tack endovascular system features adaptive sizing – which allows each Tack implant to adapt to tapering anatomy while maintaining a relatively constant radial force. This means that a single size Tack implant can be used across a wide range of vessel diameters.
The Tack endovascular system is purpose-built to repair peripheral arterial dissections following balloon angioplasty in ATK and BTK therapeutic interventions.
Purpose built
The Tack endovascular system is purpose-built to repair peripheral arterial dissections following balloon angioplasty in ATK and BTK therapeutic interventions.
Purpose built
The Tack endovascular system is purpose-built to repair peripheral arterial dissections following balloon angioplasty in ATK and BTK therapeutic interventions.
The Tack endovascular system is purpose-built to repair peripheral arterial dissections following balloon angioplasty in ATK and BTK therapeutic interventions.
Precision repair
Precision repair
Focal treatment with minimal metal treats only the area where dissections are present and avoids covering portions of healthy tissue.
Precision repair
Focal treatment with minimal metal treats only the area where dissections are present and avoids covering portions of healthy tissue.
Precision repair
Focal treatment with minimal metal treats only the area where dissections are present and avoids covering portions of healthy tissue.
Leaves behind significantly less metal than stents, preserving vessel integrity, future treatment options and—ultimately—limbs.
Adaptive sizing
Adaptive sizing
Only the Tack endovascular system features adaptive sizing – which allows each Tack implant to adapt to tapering anatomy while maintaining a relatively constant radial force. This means that a single size Tack implant can be used across a wide range of vessel diameters.
Adaptive sizing
Only the Tack endovascular system features adaptive sizing – which allows each Tack implant to adapt to tapering anatomy while maintaining a relatively constant radial force. This means that a single size Tack implant can be used across a wide range of vessel diameters.
Adaptive sizing
Only the Tack endovascular system features adaptive sizing – which allows each Tack implant to adapt to tapering anatomy while maintaining a relatively constant radial force. This means that a single size Tack implant can be used across a wide range of vessel diameters.
Only the Tack endovascular system features adaptive sizing – which allows each Tack implant to adapt to tapering anatomy while maintaining a relatively constant radial force. This means that a single size Tack implant can be used across a wide range of vessel diameters.
1. Gray WA, Cardenas JA, Brodmann M, et al. Treating Post-Angioplasty Dissection in the Femoropopliteal Arteries Using the Tack Endovascular System. JACC: Cardiovascular Interventions. 2019;12(23):2375-2384.
2. Geraghty PJ, Adams GL, Schmidt A, Lichtenberg M, Wissgott C, Armstrong EJ, Hertting K, on behalf of the TOBA II BTK Investigators. "Twelve-month results of Tack-optimized balloon angioplasty using the Tack Endovascular System in below-the-knee arteries (TOBA II BTK)." Journal of Endovascular Therapy 27.4 (2020): 626-636.
Intended use: The Tack endovascular system (4F, 1.5 mm-4.5 mm) is intended for use in mid/ distal popliteal, tibial and peroneal arteries, ranging in diameter from 1.5 mm to 4.5 mm, for the treatment of post percutaneous transluminal balloon angioplasty (PTA) dissection(s). The Tack endovascular system (6F, 3.5-6.0 mm US/ 2.5-6.0 mm EU and 4.0-8.0 mm) is intended for use in the superficial femoral and proximal popliteal arteries ranging in diameter from 3.5 mm to 6.0 mm US/ 2.5 to 6.0 mm EU and 4.0 mm to 8.0 mm for the repair of post percutaneous transluminal balloon angioplasty (PTA) dissection(s).
Contraindications for use: The Tack endovascular system is contraindicated for the following: 1. Patients with residual stenosis in the treated segment equal to or greater than 30% after PTA. 2. Tortuous vascular anatomy significant enough to prevent safe introduction and passage of the device. 3. Patients with a known hypersensitivity to nickel titanium alloy (Nitinol). 4. Patients unable to receive standard medication used for interventional procedures such as anticoagulants, contrast agents and antiplatelet therapy. Prior to using the Tack endovascular system, please review the instructions for use for a complete listing of indications, contraindications, warnings, precautions, potential adverse events and directions for use. Tack endovascular system is CE Mark authorized under EC Directive 93/42/EEC. Tack endovascular system and Tack are registered trademarks of Intact Vascular, Inc. Adaptive sizing is a trademark of Intact Vascular, Inc. Caution: U.S. Federal law restricts this device to sale by or on the order of a physician.
Door op de link te klikken, verlaat u de officiële website van Royal Philips Healthcare ("Philips"). Alle links naar websites van derden die op deze site kunnen verschijnen, zijn alleen bedoeld voor uw gemak en vertegenwoordigen op geen enkele manier enige aansluiting bij of goedkeuring van de informatie die op die gelinkte websites wordt verstrekt. Philips geeft geen verklaringen of garanties van welke aard dan ook met betrekking tot websites van derden of de daarin opgenomen informatie.
