SERAFIT
Serafit® is a braided absorbable suture, which is extremely pliable and allows a smooth passage of the thread through the tissue during suture placement with minimum sawing effect. It can be tied reliably, even in areas containing a good deal of blood or tissue secretions, and ensures knot security. SERAFIT® is available in a special form with patented suture stiffening for use in minimally invasive surgery.
Related products
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RESOLUTE INTEGRITY STENT
Resolute Onyx DES
for coronary artery disease
Resolute Onyxâ„¢ is a drug-eluting stent (DES) that’s different by design, optimised for complex PCI, and proven safe and effective in real-world, high bleeding risk patients on 1-month dual antiplatelet therapy (DAPT).1
Resolute Onyx DES is different by design to address your DES needs and a wide range of patient anatomies. It features:
- Best-in-class deliver ability
- Enhanced visibility with thinner struts
- Smooth side branch access
- Fast healing
- The broadest diameter range
Best-in-class deliverability
Single-wire design
Resolute Onyx DES is made from a single wire, which gives it a fluid range of motion and provides the flexibility needed for best-in-class deliverability.2
Sinusoid-formed wire
Helical wrap
Laser-fused
Competitive comparison
Resolute Onyx DES is more deliverable than laser-cut SYNERGYâ„¢* XD and XIENCE Skypointâ„¢*, which are stiffer.
Â
Deliverability comparison — 3.0 mm DES2
(Lower is better)
Enhanced visibility with thinner struts
Platinum-iridium core within Resolute Onyx DES increases visibility for accurate stent placement without compromising strut thickness.2Average visibility comparison2
(Higher is better)
- Cobalt alloy shell
- Platinum iridium core
Resolute Onyx cobalt alloy shell and platinum-iridum core
Smooth side branch access
Resolute Onyx DES has round struts to create a smooth passage when accessing the side branch and lower the propensity to catch during bifurcation procedures.2
Strut comparison
Rounded strut cross-section
- Resolute Onyx DES
Square strut cross-section
- SYNERGYâ„¢* DES
- XIENCEâ„¢*Â DES
Broadest diameter range
- Complex PCI requires a broad DES size matrix to match a wide range of patient anatomies.
- Resolute Onyx is the only DES with diameters ranging from 2.0 mm to 5.0 mm to treat a broad range of coronary vessel sizes.
Diameter (mm) Â Â Â Â Â Â Â Â Â Stent Length (mm) Maximum Expansion
Capabilities (MSID†) (mm)Â2.00 8 12 15 18 22 26 30 — — 3.50‡ 2.25 8 12 15 18 22 26 30 34 38 3.50‡ 2.50 8 12 15 18 22 26 30 34 38 3.50‡ 2.75 8 12 15 18 22 26 30 34 38 4.00‡ 3.00 8 12 15 18 22 26 30 34 38 4.00‡ 3.50 8 12 15 18 22 26 30 34 38 5.00‡ 4.00 8 12 15 18 22 26 30 34 38 5.00‡ 4.50 — 12 15 18 22 26 30 — — 6.00‡ 5.00 — 12 15 18 22 26 30 — — 6.00‡ PRODUCT DETAILS
2.00 RONYX20008X RONYX20012X RONYX20015X RONYX20018X RONYX20022X RONYX20026X RONYX20030X N/A N/A 2.25 RONYX22508X RONYX22512X RONYX22515X RONYX22518X RONYX22522X RONYX22526X RONYX22530X RONYX22534X RONYX22538X 2.50 RONYX25008X RONYX25012X RONYX25015X RONYX25018X RONYX25022X RONYX25026X RONYX25030X RONYX25034X RONYX25038X 2.75 RONYX27508X RONYX27512X RONYX27515X RONYX27518X RONYX27522X RONYX27526X RONYX27530X RONYX27534X RONYX27538X 3.00 RONYX30008X RONYX30012X RONYX30015X RONYX30018X RONYX30022X RONYX30026X RONYX30030X RONYX30034X RONYX30038X 3.50 RONYX35008X RONYX35012X RONYX35015X RONYX35015X RONYX35022X RONYX35026X RONYX35030X RONYX35034X RONYX35038X 4.00 RONYX40008X RONYX40012X RONYX40015X RONYX40018X RONYX40022X RONYX40026X RONYX40030X RONYX40034X RONYX40038X 4.50 N/A RONYX45012X RONYX45015X RONYX45018X RONYX45022X RONYX45026X RONYX45030X N/A N/A 5.00Â N/A RONYX50012X RONYX50015X RONYX50018X RONYX50022X RONYX50026X RONYX5 -
SPRINTER LEGEND PTCA BALLOON
SPRINTER LEGEND 1.25 BALLOON CATHETER
Super Crosser Semi compliant Balloon Dilatation Catheter (RX/OTW)
Sprinter™ Legend™ 1.25 SuperCrosser semicompliant balloon dilatation catheter delivers exceptional crossability to treat today’s challenging lesions.
With innovative crossing technologies and 57 sizes, the Sprinter™ Legend™ RX semicompliant balloon dilatation catheter provides you with the power to cross.
OVERVIEW
During difficult cases, reach for a slim Sprinterâ„¢ Legendâ„¢ 1.25 mm Super Crosser semi compliant coronary balloon catheter featuring:
- Award-winning* Zerofold technology — no wrapped material and no balloon shoulders
- Low 0.5 mm (0.020 in) crossing profile
- OTW and RX platforms
ORDERING INFORMATION
BALLOON LENGTHS 6, 10, 12, AND 15 MM
1.25 SPL12506WL SPL12510WL SPL12515WL SPL12520WL -
PTCA Balloon Ryurei
Description
Confidence in your hands
Ryureiâ„¢ has superior crossability1Â thanks to the combination of low distal profiles and Terumo’s hydrophilic M coating. The short balloon bonding and reinforced shaft1Â results in enhanced trackability1Â while maintaining excellent pushability1.
These features can increase physician’s confidence in success even during complex procedures.
CharacteristicsExcellent Pusability
The combination of flexible distal part, tapered core wire on the midshaft and the thick proximal hypotube, results in smooth and balanced transition across the entire catheter for high transmission force, resulting in excellent pushability
Superior Crossability2
Thanks to the combination of distal low profiles and the Terumo hydrophilic M-Coat, Ryurei offers low friction in crossing tight lesions
Enhanced Trackability2
With an optimal tip design and improved balloon bonding, Ryurei provides enhanced trackability, even in tortuous anatomy and difficult to navigate vessels.
General specifications
​Shaft diameter ​1.9 Fr/0.64 mm Proximal • 2.5 Fr/0.84 mm Middle • 2.4 Fr/0.79 mm to 2.7 Fr/0.89 mm (tapered) Distal (1.00 to 1.50 mm) • 2.6 Fr/0.87 mm Distal (2.00 to 4.00 mm) ​Usable length ​145 cm ​Balloon markers # ​1(Ø1.0 to Ø 1.5 mm) • 2(Ø2.0 to Ø4.0 mm) ​Nominal pressure ​6 atm / 608 kPa ​Rated burst pressure Ø1.0 – 3.0 mm=14 atm(1419kPa) • Ø3.25 – 4.0 mm = 12 atm(1216 kPa) ​Guidewire compatibility ​Maximum diameter: 0.014″ / 0.36 mm ​Lesion entry profile ​0.41 mm (Ø1.00 to Ø1.50 mm) • 0.43 mm (Ø2.00 to Ø4.00 mm) ​Coating ​Hydrophilic Item specifications
Balloon length / Product code​​ ​ ​ ​ ​ ​
Balloon Diameter 5 mm 10 mm 15 mm 20 mm 30 mm 40 mm 1.00 mm DC-RR1005HH ​1.25 mm ​DC-RR1205HH ​​DC-RR1210HH ​​DC-RR1215HH ​​DC-RR1220HH ​ ​ 1.50 mm DC-RR1505HH DC-RR1510HH DC-RR1515HH DC-RR1520HH 2.00 mm DC-RR2010HHW DC-RR2015HHW DC-RR2020HHW DC-RR2030HHW DC-RR2040HHW 2.25 mm DC-RR2210HHW DC-RR2215HHW DC-RR2220HHW 2.50 mm DC-RR2510HHW DC-RR2515HHW DC-RR2520HHW DC-RR2530HHW DC-RR2540HHW 2.75 mm DCRR2710HHW DC-RR2715HHW DC-RR2720HHW 3.00 mm DC-RR3010HHW DC-RR3015HHW DC-RR3020HHW DC-RR3030HHW DC-RR3040HHW 3.25 mm DC-RR3210HHW DC-RR3215HHW DC-RR3220HHW 3.50 mm DC-RR3510HHW DC-RR3515HHW DC-RR3520HHW DC-RR3530HHW DC-RR3540HHW 3.75 mm DC-RR3710HHW DC-RR3715HHW DC-RR3720HHW 4.00 mm DC-RR4010HHW DC-RR4015HHW DC-RR4020HHW References
1 Ryurei φ1.00-5mm compared to Tazuna 1.25-10 mm- Data on file ISCD-416-31-4
* For Ryurei Ø 1.00 mm – Ø 1.50 mm.
** For Ryurei Ø 1.00mm – 5mm ​2 Compared to Tazuna PTCA dilatation catheter
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CLOSUREFAST
ClosureFastâ„¢Â
procedureMinimally invasive thermal
treatment for vein disease
and varicose veins.
The ClosureFast procedure uses radiofrequency energy or heat to close the diseased vein, which redirects blood flow to healthy veins, relieving symptoms.Before the procedure
You will have an ultrasound imaging exam of the leg being treated. This exam is important for assessing the diseased superficial vein and planning the procedure.
During the procedure
Your doctor will discuss the procedure with you. Here is a brief summary of what to expect:
- The ClosureFast procedure is performed on an outpatient basis. Your doctor will perform the ClosureFast procedure. Using an ultrasound, your doctor will position a catheter in the diseased vein through a small opening in the skin.
- The small catheter delivers heat to the vein wall, causing it to shrink and seal the vein. Once the diseased vein is closed, blood will reroute itself to other healthy veins.
After the procedure
- You will be taken to the recovery area to rest.
- Following the procedure, your doctor will apply a simple bandage over the insertion site and will give you compression stockings to aid in the healing process. Your doctor may encourage you to walk and to refrain from extended standing and strenuous activities for a period of time. The average patient typically resumes normal activities within a few days.1,2
- Your doctor will recommend follow-up care as needed.
-
Benefits of the ClosureFast procedure
- Relief of symptoms after two days, with a noticeable improvement in one to two week
- Minimally invasive outpatient procedure
- Less pain and bruising than laser treatment
- Faster recovery than laser treatment
- Proven results with positive patient experience
Â
- Rapid recovery — on average, patients resume normal activities within a few days
- Lasting results — the only radiofrequency energy procedure with published long-term clinical data demonstrating safety and efficacy, with a 91.9% closure rate at five years.4
Adverse events can include nerve injury, hematoma, phlebitis, thrombosis, and/or pulmonary embolism.
Type of therapy
Thermal shrinkage of the vein wall with radiofrequency energy or heatInpatient or outpatient procedure
Outpatient procedureOne- versus two-leg treatment
Typically, each leg will be treated in separate appointmentsNeedle sticks required
One needle stick for vein access. Typically, 5 to 10 needle sticks for anesthesia.Â
Typical post-treatment recovery
Healing of vein access site, anesthetic needle stick sites, and also healing of ablated vein sectionCompression hose
Required for approximately one weekProcedure success rate
91.9% after five years4ClosureFast procedure FAQ
Is the ClosureFast procedure painful?
Most patients report feeling little, if any, pain during the ClosureFast procedure.3 Your doctor will give you a local or regional anesthetic to numb the treatment area.
When can I return to normal activity?
Patients treated with the ClosureFast procedure may resume normal activity more quickly than patients who undergo surgical vein stripping or laser ablation. With the ClosureFast procedure, the average patient typically resumes normal activity within a few days.2 For a few weeks following the treatment, your vein specialist may recommend a regular walking regimen and suggest you refrain from strenuous activities (heavy lifting, for example) or prolonged periods of standing.
When will my symptoms improve?
Most patients report relief of symptoms after two days, with a noticeable improvement in one to two weeks.
Is there any scarring, bruising, or swelling after the procedure?
Most patients report limited to no scarring, bruising, or swelling following the ClosureFast procedure.3
How is the ClosureFast procedure different from endovenous lasers?
Both Closure Fast and lasers use thermal technology to deliver heat into the diseased vein, but they each use a different method of delivery. Despite their similarity in using heat, a 2009 study showed that the ClosureFast procedure is associated with lower rates of pain, bruising, and complications and a faster improvement in patients’ quality of life when compared to 980 nm laser ablation.4
How is the Closure Fast procedure different from vein stripping?
During vein stripping, incisions are made in the groin and calf, and a tool is threaded through the diseased vein to pull the vein out of the leg. With the ClosureFast procedure, only one small incision is made at the insertion site and the vein is then treated and left in place. ClosureFast is a minimally invasive approach that reduces the likelihood of pain and bruising, associated with vein stripping surgery.1
Is the ClosureFast procedure covered by insurance?
Many patients have access to the ClosureFast procedure through their insurance coverage plan. Insurance companies detail access to the ClosureFast procedure and other radiofrequency ablation procedures in coverage policies for varicose veins or chronic venous insufficiency. As with all healthcare procedures, you may also have some cost associated with receiving treatment, such as a copay or coinsurance. Please reach out to your insurance company to discuss your specific plan coverage and potential costs prior to seeking treatment
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