AVANTI TRANSREDIAL SHEATH
Cordis AVANTIâ„¢+ Sheath Introducer
Smooth performance
from start to finish
The proven cannula offers reliable,
smooth performance from start to finish
• For smooth, atraumatic insertion
• Kink resistant
• Optimized catheter maneuverability
with minimal leakage
For smooth, atraumatic insertion
– Manicured tip insures smooth transition of the introducer as it crosses the miniguidewire into the artery during initial insertion
– Smooth transitions between cannula, guidewire and dilator for:
• effortless vessel entry
• increased patient comfort
• smallest possible risk for complications
Insertion Force
0
0.05
0.1
0.15
0.2
0.25
0.3
0.35
0.4
0.45
Insertion Force (lbf)
Endovascular Catalogue Numbers
5.5cm 11cm 23cm
Cannula Cannula Cannula
French Colour With Without With Without Without
size code mini-wire mini-wire mini-wire mini-wire mini-wire
4 n 402-604P 402-604X 402-604A
5 n 402-605P 402-605X 402-605A 402-605T
5.5** n 402-655X
6 n 402-606P 402-606R 402-606X 402-606A 402-606T
6.5** n 402-656X
7 n 402-607P 402-607R 402-607X 402-607A
8 n 402-608X 402-608A 402-608T
9 n 402-609X 402-609A 402-609T
10 n 402-610X 402-610A
11 n 402-611X
Smooth Performance from Start to Finish
**
5F MS = Mid-Size = 5.5F
6F MS = Mid-Size = 6.5F
French Colour Mini-wire With Without
size code (inch) mini-wire mini-wire
4 n .035 504-604X 504-604A
5 n .038 504-605X 504-605A
5.5** n .038 504-655X*
6 n .038 504-606X 504-606A
6.5** n .038 504-656X* 504-656A*
7 n .038 504-607X 504-607A
7.5** n .038 504-657X*
8 n .038 504-608X 504-608A
8.5** n .038 504-658X*
9 n .038 504-609X 504-609A
10 n .038 504-610X 504-610A
11 n .038 504-611X
* Monitoring sheath: provides slightly larger ID for pressure monitoring or side port aspiration with a catheter in place; they are one-half French size larger in size
** 5F MS = Mid-Size = 5.5F
6F MS = Mid-Size = 6.5F
7F MS = Mid-Size = 7.5F
8F MS = Mid-Size = 8.5F
** 6F MS= Mid-Size=6.5FC
French Colour Dilator usable With Without
size code (cm) obturator obturator
4 n 30 504-604T
5 n 30 504-605T
6 n 30 504-606D 504-606T
6.5** n 30 504-656T*
7 n 30 504-607D 504-607T
8 n 30 504-608D 504-608T
10 n 30 504-610T
11 n 30 504-611TC
French Colour Mini-wire Catalogue
size code (inch) number
6 n .038 504-606V
7 n .038 504-607V
8 n .038 504-608V
French Colour Mini-wire Catalogue
size code (inch) number
4 n .035 504-604P
5 n .038 504-605P
6 n .038 504-606P
French Colour Mini-wire Catalogue
size code (inch) number
4 n .021 504-604S
5 n .021 504-605S
6 n .021 504-606S
French Colour Wire acceptance Catalogue Wire acceptance Catalogue
size code (inch) number (inch) number
4 n .021 504-614Z .021 70 cm 504-624Z
5 n .021 504-615Z .021 70 cm 504-625Z
6 n .021 504-616Z .021 70 cm 504-626Z
AVANTI TRANSREDIAL SHEATH
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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
-
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 years4
ClosureFast 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
-
FINECROSS Microcatheter
FINECROSS® MG Coronary Micro-Guide Catheter
Product Code Catheter Length Distal Hydrophilic Coating Distal Outer Diameter Proximal Outer Diameter Distal Inner Diameter Proximal Inner Diameter Recommended Guidewire Size 35-1430 130cm 70cm 1.8Fr. (0.60mm) 2.6 Fr. (0.87mm) 0.018″ (0.45mm) 0.021″ (0.55mm) 0.014″ (0.36mm) 35-1450 150cm 90cm 1.8Fr. (0.60mm) 2.6 Fr. (0.87mm) 0.018″ (0.45mm) 0.021″ (0.55mm) 0.014″ (0.36mm) PRODUCT OVERVIEW
Coronary microguide catheter for integration of optimal guidewire support, superior trackability and crossability.1,2

TAPERED STAINLESS STEEL BRAID CONSTRUCTION FOR OPTIMAL GUIDEWIRE SUPPORT
FINECROSS MG stainless steel braid construction is designed to provide strength, responsiveness and support for improved pushability to access and cross complex lesions.
13cm FLOPPY DISTAL SEGMENT FOR SUPERIOR TRACKABILITY1
The distal 13 cm is ultra flexible for improved trackability around tight bends and tortuous anatomy.The floppy distal segment is designed to be atraumatic and provide an optimal balance between trackability and safety while navigating through the tortuous anatomy.1
TAPERED OUTER DIAMETER FOR SUPERIOR CROSSABILITY1,2
The outer diameter of the stainless steel shaft tapers from a proximal 2.6Fr. to a distal 1.8Fr. designed for improved crossability and guidewire handling.1,2
DOCUMENTS







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