Paris Baguette Singapore Pte Ltd.

Ultimaster Nagomi™


Navigate the complexities of every procedure for optimal outcomes for/with every patient​​

You can tackle any procedure with ease, adapting and conforming to the length and contours of vessels. Even in the most challenging anatomy, smooth trackability and reliable overexpansion allow for excellent maneuverability. Ultimaster Nagomi provides the versatility and flexibility you need to deliver the best possible results.1-3

As the newest solution in the Ultimaster™ product range — now with the largest size line-up — we build on its clinical legacy and expertise, adding a new level of innovation to your practice.1-3

Go anywhere with Ultimaster Nagomi™.

CONTACT A REPRESENTATIVE

Characteristics

Improved Stent Design4.5

  • 3 platforms specifically designed to meet the needs of each vessel size4,5
  • Strut & band width shortened to help increase flexibility (for Ø2.00mm to Ø2.50mm stents)4-6
  • New 10-crown design in the large vessel :
    • to ensure better apposition even in large bifurcations, including left main trunk4,5,7
    • allows a better expansion capability with a uniform vessel coverage compared to an 8-crown design4,5,8,9

Larger Size Line-up11

  • The largest size line-up in the Ultimaster Family, from Φ2.00 to Φ4.50mm and 9 to 50mmlength to treat a broader range of lesions4,5,8
  • New 44 & 50m lengths, for optimal sizing in long lesions4,5

Greater Overexpansion Capability11

  • 10-crown design for a better expansion in large vessels4,5,8
  • Optimized overexpansion capability, up to 6.25 mm (for Ø3.50mm to Ø4.50mm stents)8

Excellent Deliverability11

  • New hydrophilic coating for enhanced deliverability10,11
  • New balloon with a nominal pressure of 11 atm for a better apposition7,12
  • Increased catheter inner lumen for fast deflation time13,14

Inherited Drug and Polymer

Inherited abluminal gradient bioresorbable coating to maintain polymer integrity even when overexpanded, allowing for an optimized drug dose of sirolimus (3.9 μg/mm of stent)4,5,15,16, simultaneous polymer resorption and drug release within 3-4 months.

Ultimaster Nagomi™ is building on the Heritage of Strong Clinical Evidence of the Ultimaster™ Stent Family22

Preparation

Video instructions

Clinical evidence

Abbreviated Antiplatelet Therapy After Coronary Stenting in Patients with Myocardial Infarction at High Bleeding Risk

C. Smits et al J Am Coll Cardiol. 2022

Duration of antiplatelet therapy after complex percutaneous coronary intervention in patients at high bleeding risk : a MASTER DAPT trial sub-analysis.

Valgimigli et al. Eur Heart J. 2022

General specifications

Stent specifications

Stent design Open cell
Stent material Cobalt Chromium L605
Strut thickness 80 μm
Drug Sirolimus
Drug dose 3.9 μg/mm stent length
Polymer Poly (DL-lactide-co-caprolactone)
Drug coating Abluminal & gradient
Polymer degradation time and drug release 3-4 months

Delivery system specifications

Guidewire compatibility 0.014’’ (0.36 mm)
Nominal pressure 11 atm
Rated burst pressure 16 atm
Entry profile 0.018’’ (0.45 mm)
Coating Hydrophilic – Distal shaft
Minimum guide catheter 5 Fr for Ø 2.00 – Ø 4.00 mm (0.056’’/1.42 mm) 6 Fr for Ø 4.50 mm (0.071’’/1.80 mm)​
Usable length 144 cm

Item specifications

Length (mm) Diameter (mm)
2.00 2.25 2.50 2.75 3.00 3.50 4.00 4.50
9 DE-RS2009ASM DE-RS2209ASM DE-RS2509ASM DE-RS2709ASM DE-RS3009ASM DE-RS3509ASM DE-RS4009ASM DE-RS4509ASM
12 DE-RS2012ASM DE-RS2212ASM DE-RS2512ASM DE-RS2712ASM DE-RS3012ASM DE-RS3512ASM DE-RS4012ASM DE-RS4512ASM
15 DE-RS2015ASM DE-RS2215ASM DE-RS2515ASM DE-RS2715ASM DE-RS3015ASM DE-RS3515ASM DE-RS4015ASM DE-RS4515ASM
18 DE-RS2018ASM DE-RS2218ASM DE-RS2518ASM DE-RS2718ASM DE-RS3018ASM DE-RS3518ASM DE-RS4018ASM DE-RS4518ASM
21 DE-RS2021ASM DE-RS2221ASM DE-RS2521ASM DE-RS2721ASM DE-RS3021ASM DE-RS3521ASM DE-RS4021ASM DE-RS4521ASM
24 DE-RS2024ASM DE-RS2224ASM DE-RS2524ASM DE-RS2724ASM DE-RS3024ASM DE-RS3524ASM DE-RS4024ASM DE-RS4524ASM
28 DE-RS2028ASM DE-RS2228ASM DE-RS2528ASM DE-RS2728ASM DE-RS3028ASM DE-RS3528ASM DE-RS4028ASM DE-RS4528ASM
33 DE-RS2033ASM DE-RS2233ASM DE-RS2533ASM DE-RS2733ASM DE-RS3033ASM DE-RS3533ASM DE-RS4033ASM DE-RS4533ASM
38 DE-RS2038ASM DE-RS2238ASM DE-RS2538ASM DE-RS2738ASM DE-RS3038ASM DE-RS3538ASM DE-RS4038ASM DE-RS4538ASM
44 DE-RS2044ASM DE-RS2244ASM DE-RS2544ASM DE-RS2744ASM DE-RS3044ASM DE-RS3544ASM DE-RS4044ASM DE-RS4544ASM
50 DE-RS2050ASM DE-RS2250ASM DE-RS2550ASM DE-RS2750ASM DE-RS3050ASM DE-RS3550ASM DE-RS4050ASM DE-RS4550ASM
Post-dilation limit 3.50 mm
4.50 mm
6.25 mm

References

  1. Data on file
  2. Wijns W et al. EuroIntervention 2018;14:e343-55
  3. Cimci M et al. Heart 2022;doi: 10.1136/heartjnl-2021-320116
  4. Technical documentation, PS-0084
  5. Product Standard, PS-1084
  6. Internal test report, LMF-0000041-RAFR-001-1162
  7. Internal test report, LMF-0000041-RAFR-001-1070
  8. Ultimaster Nagomi™ Instructions for Use.
  9. Hikichi Y, EBC 2022 (https://youtu.be/hJg2SE4GzPU?t=2967)
  10. Internal test report, LMF-0000041-RAFR-001-1202
  11. Internal test report, LMF-0000041-RAFR-001-1159
  12. Internal test report, LMF-0000041-RAFR-001-1184
  13. Internal test report, LMF-0000041-RAFR-001-1044
  14. Internal bench test, DC-0109545
  15. Barbato E et al. EuroIntervention 2015;11:541–8
  16. Saito N et al. Med Devices 2016;9:33–45
  17. PS-6084B
  18. Chevalier B et al. Circ Cardiovasc Interv 2017;10:pii:e004801.
  19. Wijns W et al. EuroIntervention 2018;14:e343–51.
  20. Cimci M et al. Heart 2022 108:1310-1318
  21. Valgimigli M et al. N Engl J Med 2021;385:1643-1655; 11
  22. We have proven equivalency according to the definition in MDR using the guidance on equivalency (MDCG 2020-5)