Pantera™ Pro
Coronary Dilatation
Catheter
For dilatation of coronary artery
or bypass graft stenosis*
Excellent Pushability
Excels in Challenging Cases.
The reduced distal shaft profile lowers friction when using two balloons in a 6F guiding catheter.**
| Proximal Shaft | |
|---|---|
| Design | Hypotube design |
| Diameter | 2.0F |
| Shaft markers | 92 cm and 102 cm from tip |
| Distal shaft | |
|---|---|
| Guiding catheter | 5F (min. I.D. 0.056”/1.42 mm) |
| Guide wire diameter | 0.014” |
| Lesion entry profile | 0.017” |
| Usable length | 140 cm |
| Distal shaft length | 29 cm |
| Balloon material | SCP (Semi Crystalline Co-Polymer) |
| Balloon folding | 1.25 - 1.5 mm: Two-fold; 2.0 - 4.0 mm: Tri-fold |
| Balloon markers | Platinum-iridium 1.25 - 1.5 mm one mid-marker; 2.0 - 4.0 mm two markers at balloon ends |
| Coating distal shaft | Hydrophilic (end of balloon to Guide Wire exit port) |
| Balloon and tip coating | 1.25 - 2.0 mm: Hydrophilic; 2.50 - 4.0 mm: Hydrophobic |
| Kissing balloon technique | 6F guiding catheter (min. I.D. 0.070” / 1.78 mm), up to 3.5 mm |
| Diameter | 2.6F (1.25 - 2.0 mm); 2.7F (2.5 - 3.5 mm); 2.9F (4.0 mm) |
| Inflation Pressure | Balloon Diameter (mm) | ||||||||
|---|---|---|---|---|---|---|---|---|---|
| atm | (kPa) | 1.25 | 1.5 | 2.0 | 2.5 | 3.0 | 3.5 | 4.0 | |
| 6 | (608) | 1.22 | 1.46 | 1.97 | 2.41 | 3.00 | 3.53 | 3.83 | |
| Nominal Pressure (NP) | 7 | (709) | 1.24 | 1.49 | 2.01 | 2.49 | 3.08 | 3.62 | 3.95 |
| 8 | (811) | 1.26 | 1.53 | 2.05 | 2.58 | 3.17 | 3.72 | 4.07 | |
| 9 | (912) | 1.27 | 1.56 | 2.09 | 2.66 | 3.24 | 3.80 | 4.18 | |
| 10 | (1013) | 1.30 | 1.60 | 2.12 | 2.72 | 3.31 | 3.87 | 4.28 | |
| 11 | (1115) | 1.31 | 1.63 | 2.16 | 2.79 | 3.37 | 3.93 | 4.36 | |
| 12 | (1216) | 1.33 | 1.66 | 2.18 | 2.84 | 3.42 | 3.97 | 4.43 | |
| 13 | (1317) | 1.35 | 1.69 | 2.21 | 2.88 | 3.45 | 4.02 | 4.49 | |
| Rated Burst Pressure (RBP) | 14 | (1419) | 1.37 | 1.72 | 2.23 | 2.93 | 3.50 | 4.06 | 4.55 |
| 15 | (1520) | 1.39 | 1.74 | 2.26 | 2.97 | 3.54 | 4.10 | 4.60 | |
| Balloon Ø | Catheter Length 140 cm, Balloon Length | ||||||
|---|---|---|---|---|---|---|---|
| 6 mm | 10 mm | 15 mm | 20 mm | 25 mm | 30 mm | ||
| 1.25 mm | 393289 | 393291 | 393298 | 393305 | - | - | |
| 1.50 mm | 393290 | 393292 | 393299 | 393306 | - | - | |
| 2.00 mm | - | 393293 | 393300 | 393307 | 393312 | 393317 | |
| 5F | 2.50 mm | - | 393294 | 393301 | 393308 | 393313 | 393318 |
| 3.00 mm | - | 393295 | 393302 | 393309 | 393314 | 393319 | |
| 3.50 mm | - | 393296 | 393303 | 393310 | 393315 | 393320 | |
| 4.00 mm | - | 393297 | 393304 | 393311 | 393316 | 393321 | |
*The Pantera™ Pro Coronary Dilatation Catheter is indicated for balloon dilatation of the stenotic portion of a coronary artery or bypass graft stenosis for the purpose of improving myocardial perfusion. The Pantera™ Pro Coronary Dilatation Catheter (balloon diameter 2.0 – 4.0 mm) is also indicated for post-delivery expansion of balloon expandable stents.
** Any combination of two diameters not larger than 3.5 mm within a 6F guiding catheter with a minimal inner diameter of 0.070”/1.78 mm.
REFERENCES:
1.Testing conducted by the Institute for Implant Technology and Biomaterials and paid for by BIOTRONIK AG, now Teleflex. Test data may not be indicative of clinical performance.
CAUTION: Federal Law (U.S.A.) restricts this device to sale or use by or on the order of a physician.
Teleflex, the Teleflex logo, and Pantera are trademarks or registered trademarks of Teleflex Incorporated or its affiliates in the U.S. and/or other countries. Please see the Instructions for Use for a complete listing of the indications, contraindications, warnings and precautions. Information in this material is not a substitute for the product Instructions for Use. Not all products may be available in all countries. Please contact your local representative. All other trademarks marked with a TM are the property of their respective owners and are solely used for identification purposes and do not imply any affiliation, endorsement, or ownership by Teleflex Incorporated or its affiliates.
© 2026 Teleflex Incorporated. All rights reserved. MC-011823 Rev 0. Revised: 05/2026.