Pantera™ LEO
PTCA Catheter
Non-Compliant High
Pressure Balloon
Catheter
For coronary stent post-dilatation and dilatation of a
coronary artery or bypass graft stenosis*
Strength: Compliance
Accuracy: Precise Post-Dilatation.
Short balloon shoulders reduce longitudinal balloon growth, minimizing potential for vessel trauma outside treatment area.
Patchwork coating
Partly coated when inflated – designed to avoid slippage during inflation.
| Proximal Shaft | |
|---|---|
| Design | Hypotube design |
| Diameter | 2.0F |
| Shaft markers | 92 cm and 102 cm from tip |
| Coating | Hydrophobic |
| Distal shaft | |
|---|---|
| Guiding catheter | 5F (min. I.D. 0.056”) |
| Guide wire diameter | 0.014” |
| Lesion entry profile | 0.018” |
| Usable length | 145 cm |
| Distal shaft length | 34 cm |
| Balloon material | SCP (Semi Crystalline Polymer) |
| Balloon folding | 3-fold |
| Balloon markers | Platinum-Iridium |
| Coating | Hydrophilic (end of balloon to guide wire exit port) Hydrophobic (balloon and tip) |
| Diameter | 2.6F (2.0 - 3.75 mm) 2.7F (4.0 - 5.0 mm) |
| Inflation Pressure | Balloon Diameter (mm) | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| atm | 2.0 | 2.25 | 2.5 | 2.75 | 3.0 | 3.25 | 3.5 | 3.75 | 4.0 | 4.5 | 5.0 | ||
| Nominal Pressure (NP) | 14 | 2.0 | 2.25 | 2.50 | 2.75 | 3.00 | 3.25 | 3.50 | 3.75 | 4.00 | 4.50 | 5.00 | |
| 15 | 2.01 | 2.26 | 2.51 | 2.76 | 3.01 | 3.27 | 3.52 | 3.77 | 4.02 | 4.52 | 5.02 | ||
| 16 | 2.02 | 2.27 | 2.52 | 2.77 | 3.03 | 3.28 | 3.54 | 3.80 | 4.04 | 4.53 | 5.04 | ||
| 17 | 2.03 | 2.28 | 2.54 | 2.79 | 3.04 | 3.30 | 3.55 | 3.82 | 4.06 | 4.55 | 5.05 | ||
| Rated Burst Pressure (RBP) | 18 | 2.04 | 2.30 | 2.55 | 2.80 | 3.06 | 3.32 | 3.57 | 3.84 | 4.08 | 4.56 | 5.07 | |
| 19 | 2.05 | 2.31 | 2.56 | 2.81 | 3.07 | 3.33 | 3.59 | 3.87 | 4.10 | 4.58 | 5.09 | ||
| Rated Burst Pressure (RBP) | 20 | 2.05 | 2.32 | 2.57 | 2.83 | 3.09 | 3.35 | 3.61 | 3.89 | 4.12 | 4.60 | 5.11 | |
| Balloon DIAMETER | Balloon Length | |||||
|---|---|---|---|---|---|---|
| 8 mm | 12 mm | 15 mm | 20 mm | 30 mm | ||
| 2.00 mm | 366991 | 367002 | 367013 | 367024 | 367035 | |
| 2.25 mm | 366992 | 367003 | 367014 | 367025 | 367036 | |
| 2.50 mm | 366993 | 367004 | 367015 | 367026 | 367037 | |
| 2.75 mm | 366994 | 367005 | 367016 | 367027 | 367038 | |
| 3.00 mm | 366995 | 367006 | 367017 | 367028 | 367039 | |
| 5F | 3.25 mm | 366996 | 367007 | 367018 | 367029 | 367040 |
| 3.50 mm | 366997 | 367008 | 367019 | 367030 | 367041 | |
| 3.75 mm | 366998 | 367009 | 367020 | 367031 | 367042 | |
| 4.00 mm | 366999 | 367010 | 367021 | 367032 | 367043 | |
| 4.50 mm | 367000 | 367011 | 367022 | 367033 | 367044 | |
| 5.00 mm | 367001 | 367012 | 367023 | 367034 | 367045 | |
* Indicated for balloon dilatation of the stenotic portion of a coronary artery or bypass graft stenosis for the purpose of improving myocardial perfusion and for post-dilatation of coronary stents.
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.
2. Average growth from NP to RBP for 2.0 – 5.0 mm diameters
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-011822 Rev 0. Revised: 05/2026.