PTS-X™ Sizing Balloon Catheter
Recommended for use in those patients with cardiovascular defects wherein accurate measurement of the defect is important to select the appropriately sized occluder device.
- Xtra high inner lumen strength
- Xtra fast guidewire movement (even with balloon inflated)
- Increased pushability from new braided inner tubing
- Radiopaque inner tubing
- Specifications
-
Product specifications
Ballon
Diameter
(MM)Ballon
Lengte
(CM)Introducer
Afmeting
(FR)Schacht
Afm.
(FR)Bruikbare
Lengte
(CM)Voer-
draad
(Inches)Nominale
Ontlading
(ATM)Catalogus
Nr.10.0 1.0 6 6 80 0.035 2.5 PTSX101 10.0 2.0 6 6 80 0.035 2.5 PTSX102 10.0 3.0 6 6 80 0.035 2.5 PTSX103 10.0 1.0 6 6 110 0.035 2.5 PTSX104 10.0 2.0 6 6 110 0.035 2.5 PTSX105 10.0 3.0 6 6 110 0.035 2.5 PTSX106 12.0 2.0 6 6 80 0.035 2.0 PTSX122 12.0 3.0 6 6 80 0.035 2.0 PTSX123 12.0 2.0 6 6 110 0.035 2.0 PTSX124 12.0 3.0 6 6 110 0.035 2.0 PTSX125 15.0 2.0 6 6 80 0.035 2.0 PTSX152 15.0 3.0 6 6 80 0.035 2.0 PTSX153 15.0 4.0 6 6 80 0.035 2.0 PTSX154 15.0 2.0 6 6 110 0.035 2.0 PTSX155 15.0 3.0 6 6 110 0.035 2.0 PTSX156 15.0 4.0 6 6 110 0.035 2.0 PTSX157 20.0 3.0 8 8 80 0.035 1.5 PTSX203 20.0 4.0 8 8 80 0.035 1.5 PTSX204 20.0 3.0 8 8 110 0.035 1.5 PTSX205 20.0 4.0 8 8 110 0.035 1.5 PTSX206 25.0 3.0 8 8 80 0.035 1.5 PTSX253 25.0 4.0 8 8 80 0.035 1.5 PTSX254 25.0 3.0 8 8 110 0.035 1.5 PTSX255 25.0 4.0 8 8 110 0.035 1.5 PTSX256 30.0 3.0 8 8 80 0.035 1.0 PTSX303 30.0 4.0 8 8 80 0.035 1.0 PTSX304 30.0 5.0 8 8 80 0.035 1.0 PTSX305 30.0 3.0 8 8 110 0.035 1.0 PTSX306 30.0 4.0 8 8 110 0.035 1.0 PTSX307 30.0 5.0 8 8 110 0.035 1.0 PTSX308 35.0 3.0 9 8 110 0.035 1.0 PTSX357 35.0 4.0 9 8 110 0.035 1.0 PTSX358 35.0 5.0 9 8 110 0.035 1.0 PTSX359 35.0 6.0 9 8 110 0.035 1.0 PTSX360 40.0 3.0 9 8 80 0.035 0.5 PTSX403 40.0 4.0 9 8 80 0.035 0.5 PTSX404 40.0 5.0 9 8 80 0.035 0.5 PTSX405 40.0 6.0 9 8 80 0.035 0.5 PTSX406 40.0 3.0 9 8 110 0.035 0.5 PTSX407 40.0 4.0 9 8 110 0.035 0.5 PTSX408 40.0 5.0 9 8 110 0.035 0.5 PTSX409 40.0 6.0 9 8 110 0.035 0.5 PTSX410 The devices listed have CE mark approval. Any customer or distributor outside of the EU will be subject to their individual country's regulations in regards to the importation and sale of these products.
This publication could include technical or other inaccuracies or typographical errors. Changes are periodically added to the information herein; these changes will be incorporated in the new editions of the publication. NuMED Incorporated may make improvements and/or changes in the product(s) and/or the program(s) described in this publication at any time.