Cache Test Div

Technical data

 
STENT
Stent Material Cobalt chromium, L-605
Passive coating proBIO amorphous silicon carbide
Active coating BIOlute bioabsorbable drug matrix consisting of sirolimus and polymer poly-l-lactide (PLLA)
Nominal drug content 1.4 μg/mm2
Delivery system
Catheter type Fast-exchange
Recommended guide catheter 5F (min. I.D.Δ ≥ 0.056“)
Guide wire diameter 0.014” (0.36 mm)
Usable catheter length 140 cm
Balloon material Polymer
Coating (distal shaft) Hydrophilic coating
Marker bands Two platinum-iridium markers
Proximal shaft diameter 2.0F
Distal shaft diameter ø 2.25-3.5 mm: 2.6F

ø 4.0 mm: 2.8F
Nominal pressure (NP) Ø 2.25-2.75, 3.5-4.0 mm: 7 atm

Ø 3.0 mm: 8 atm
Rated burst pressure (RBP) 16 atm

 

Ordering information

Stent ø (mm) Catheter length 140 cm Stent length (mm)
  9 13 15 18 22 26 30 35 40
2.25 401729 401735 401741 401747 401753 401759 401765 - -
2.50 401730 401736 401742 401748 401754 401760 401766 404667 404673
2.75 401731 401737 401743 401749 401755 401761 401767 404668 404674
3.00 401732 401738 401744 401750 401756 401762 401768 404669 404675
3.50 401733 401739 401745 401751 401757 401763 401769 404670 404676
4.00 401734 401740 401746 401752 401758 401764 401770 404671 404677

 

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​​​​​​​ΔI.D. = Inner Diameter​​​​​​​

Orsiro, proBIO and BIOlute are trademarks or registered trademarks of the BIOTRONIK Group of Companies.  

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Orsiro DES is indicated for improving coronary luminal diameter in patients, including those with diabetes mellitus, with symptomatic heart disease, stable angina, unstable angina, non-ST elevation myocardial infarction or documented silent ischemia due to atherosclerotic lesions in the native coronary arteries with a reference vessel diameter of 2.25 mm to 4.0 mm and a lesion length of ≤ 36 mm.