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Only IN.PACT Admiral and IN.PACT 018 DCBs release the drug into tissue through the restenotic window.
Duration of paclitaxel in tissue‡
Days after index procedure
The safety and effectiveness of the IN.PACT Admiral DCB (0.035 in guidewire compatible), as established in the clinical studies that were performed primarily via femoral access, can be considered supportive for the IN.PACT 018 DCB. The IN.PACT 018 DCB has not been evaluated in a clinical study.
IN.PACT DCBs are coated with a combination of paclitaxel and an excipient, urea. The unique formulation allows rapid and efficient delivery of drug to the vessel wall.
Watch a video to see how our DCBs work.
IN.PACT Admiral DCB Mechanism of Action - (03:44)
See how the IN.PACT Admiral drug-coated balloon works.
More information (see more)
Less information (see less)
Features |
Specifications |
|
---|---|---|
IN.PACT Admiral DCB |
IN.PACT 018 DCB |
|
Guidewire compatibility |
0.035 in |
0.018 in |
Catheter design |
Over-the-wire (OTW) |
Over-the-wire (OTW) |
Catheter lengths |
80 and 130 cm |
130 and 200 cm |
Balloon diameters |
4.0 to 7.0 mm |
4.0 to 7.0 mm |
Balloon lengths |
40, 60, 80, 120, 150, 200, 250 mm¶ |
40, 60, 80, 100, 120, 150 mm |
Balloon fold configurations |
4.0 mm: 3 folds |
4.0 mm: 3 folds |
Paclitaxel drug dose |
3.5 µg/mm2 |
3.5 µg/mm2 |
Excipient |
Urea |
Urea |
Model number |
Balloon diameter (mm) |
Balloon length (mm) |
Recommended introducer sheath (F) |
Nominal pressure (atm) |
RBP (atm) |
---|---|---|---|---|---|
IPU04004013P |
4.0 |
40 |
5 |
8 |
10 |
IPU04006013P |
4.0 |
60 |
5 |
8 |
10 |
IPU04008013P |
4.0 |
80 |
5 |
8 |
10 |
IPU04010013P |
4.0 |
100 |
5 |
8 |
10 |
IPU04012013P |
4.0 |
120 |
5 |
8 |
10 |
IPU04015013P |
4.0 |
150 |
5 |
8 |
10 |
IPU05004013P |
5.0 |
40 |
5 |
8 |
10 |
IPU05006013P |
5.0 |
60 |
5 |
8 |
10 |
IPU05008013P |
5.0 |
80 |
5 |
8 |
10 |
IPU05010013P |
5.0 |
100 |
5 |
8 |
10 |
IPU05012013P |
5.0 |
120 |
5 |
8 |
10 |
IPU05015013P |
5.0 |
150 |
5 |
8 |
10 |
IPU06004013P |
6.0 |
40 |
5 |
8 |
10 |
IPU06006013P |
6.0 |
60 |
5 |
8 |
10 |
IPU06008013P |
6.0 |
80 |
5 |
8 |
10 |
IPU06010013P |
6.0 |
100 |
5 |
8 |
10 |
IPU06012013P |
6.0 |
120 |
5 |
8 |
10 |
IPU06015013P |
6.0 |
150 |
5 |
8 |
10 |
IPU07004013P |
7.0 |
40 |
6 |
8 |
10 |
IPU07006013P |
7.0 |
60 |
6 |
8 |
10 |
IPU07008013P |
7.0 |
80 |
6 |
8 |
10 |
Model number |
Model number |
Balloon diameter (mm) |
Balloon length (mm) |
Recommended introducer sheath (F) |
Nominal pressure (atm) |
RBP (atm) |
---|---|---|---|---|---|---|
ADM 040 040 08P |
ADM 040 040 13P |
4.0 |
40 |
5 |
8 |
14 |
ADM 040 060 08P |
ADM 040 060 13P |
4.0 |
60 |
5 |
8 |
14 |
ADM 040 080 08P |
ADM 040 080 13P |
4.0 |
80 |
5 |
8 |
14 |
ADM 040 120 08P |
ADM 040 120 13P |
4.0 |
120 |
5 |
8 |
14 |
ADM 040 150 08P |
ADM 040 150 13P |
4.0 |
150 |
5 |
8 |
14 |
ADM 050 040 08P |
ADM 050 040 13P |
5.0 |
40 |
6 |
8 |
14 |
ADM 050 060 08P |
ADM 050 060 13P |
5.0 |
60 |
6 |
8 |
14 |
ADM 050 080 08P |
ADM 050 080 13P |
5.0 |
80 |
6 |
8 |
14 |
ADM 050 120 08P |
ADM 050 120 13P |
5.0 |
120 |
6 |
8 |
14 |
ADM 050 150 08P |
ADM 050 150 13P |
5.0 |
150 |
6 |
8 |
14 |
ADM 060 040 08P |
ADM 060 040 13P |
6.0 |
40 |
6 |
8 |
14 |
ADM 060 060 08P |
ADM 060 060 13P |
6.0 |
60 |
6 |
8 |
14 |
ADM 060 080 08P |
ADM 060 080 13P |
6.0 |
80 |
6 |
8 |
14 |
ADM 060 120 08P |
ADM 060 120 13P |
6.0 |
120 |
6 |
8 |
14 |
ADM 060 150 08P |
ADM 060 150 13P |
6.0 |
150 |
6 |
8 |
14 |
ADM 070 040 08P |
ADM 070 040 13P |
7.0 |
40 |
7 |
8 |
14 |
ADM 070 060 08P |
ADM 070 060 13P |
7.0 |
60 |
7 |
8 |
14 |
ADM 070 080 08P |
ADM 070 080 13P |
7.0 |
80 |
7 |
8 |
14 |
Find the technical manuals in the Medtronic Manual Library, in the product labeling supplied with each device, or by calling Medtronic at 763-526-7890.
Reach a Medtronic sales rep
Contact us here
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The safety and effectiveness of the IN.PACT Admiral DCB (0.035 in guidewire compatible), as established in the clinical studies that were performed primarily via femoral access, can be considered supportive for the IN.PACT 018 DCB. The IN.PACT 018 DCB has not been evaluated in a clinical study.
™Third-party brands are trademarks of their respective owners. All other brands are trademarks of a Medtronic company.
Data on file with Medtronic.
Data comes from different individual studies and may differ in a head-to-head comparison, and therefore may not be predictive of clinical results.
Primary patency not assessed after three years.
List of publications on file with Medtronic.
120, 150, 200, and 250 mm lengths are not offered on the 7.0 mm diameter balloon.
Laird JA, Schneider PA, Jaff MR, et al. Long-Term Clinical Effectiveness of a Drug-Coated Balloon for the Treatment of Femoropopliteal Lesions. 5-year results from the IN.PACT SFA Trial. Circ Cardiovasc Interv. June 2019;12(6):e007702.
Tepe G. 5-year results from the IN.PACT Global Study Prespecified Cohorts: ISR, CTO and Long Lesions. Presented at VIVA, 2021.
PMA P140010: Summary of safety and effectiveness data. FDA. Available at: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?id=p140010. Accessed September 26, 2022.
PMA P190019: Summary of safety and effectiveness data. FDA. Available at: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?id=P190019. Accessed September 26, 2022.
Yazdani SK, Pacheco E, Nakano M, et al. Vascular, downstream, and pharmacokinetic responses to treatment with a low dose drug-coated balloon in a swine femoral artery model. Catheter Cardiovasc Interv. January 1, 2014;83(1):132-140.
PMA P160049: Summary of safety and effectiveness data. FDA. Available at: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?id=P160049. Accessed September 26, 2022.