(OPTEASE/TRABEASE) IVC FILTER
OPTEASE Retrievable Vena Cava Filters are an innovative option for prevention of recurrent pulmonary embolism.
Product Description
OPTEASE Retrievable Vena Cava Filters are an option for prevention of pulmonary embolism.
- Dual-layer filtration for easier clot capture and prevention of pulmonary embolism
- Fixation barb minimizes migration to maintain clot capture efficiency
- Caudal filter retrieval hook for easy retrieval with any appropriate endovascular snare
- Caval coverage up to 30 mm
- Nitinol technology No waiting period is required between filter placement and having an MRI
One OPTEASE Retrievable Vena Cava Filter kit provides more options:
- 90cm kit allows filter delivery through six entry sites (right and left femoral, jugular, and antecubital veins)
- 55cm kit allows filter delivery through four entry sites (right and left femoral and jugular veins)
- No need to change systems when changing access sites.
Cordis Optease & trabease IVC Filter Injuries Cordis Corporation makes the Optepse and Trapease IVC filters, which are designed to prevent pulmonary embolisms Unfortunately, recent studies have found alarming rates of filter fracture, perforation, migration, and tilting when the filters are not removed after a few months.
Cordis Corporation makes two IVC filters, the OptEase and TrapEase. These devices are implanted in the inferior vena cava (IVC) to block blood clots from the leg before they cause pulmonary embolism.
The Cordis Trabease is a permanent vena cava filter, which was approved by the FDA in 2001.
Related products
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ACT CARTRIDGE (HR-ACT)
Medtronic 402-03 ACT PLUS Disposable Test Cartridges 2-Channel Test Cartridges, High Range Activated Clotting Time (HR ACT) – Fresh whole blood test for CV surgery, PTCA, or vascular surgery, Box of 50
SKU:402-03Weight:3.00 LBSAvailability:2-3 Business daysShipping:Calculated at checkoutQuantity:Product Description
Medtronic 402-03 ACT PLUS Disposable Test Cartridges 2-Channel Test Cartridges, High Range Activated Clotting Time (HR ACT) – Fresh whole blood test for CV surgery, PTCA, or vascular surgery, Box of 50Â
                   ACT PLUS Disposable Test Cartridges 2-Channel Test Cartridges
402-01 Low Range Activated Clotting Time (LR ACT) – Fresh whole blood test for therapeutic heparin monitoring, post-angioplasty or dialysis 50 per box 402-02 Recalcified Activated Clotting Time (RACT) – For use with citrated whole blood samples at concentrations of 0.0 – 1.5 u/mL 50 per box 402-03 High Range Activated Clotting Time (HR ACT) – Fresh whole blood test for CV surgery, PTCA, or vascular surgery 50 per box 402-07 Heparinase Test Cartridge (HTC) – Fresh whole blood test used to identify the presence of heparin in the patient’s blood sample 20 per box -
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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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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GUIDING CATHETER EKARI
Product Overview
IMPROVED BACK UP SUPPORT*1
Catheter designed to use contralateral wall resulting in enhanced back-up support.
UNIVERSAL SHAPE (IKARI LEFT)Â *2
Offer capability of accessing the right and left coronary arteries, potentially avoiding catheter exchanges.
DESIGN FOR SAFETY
Soft tip to reduce damage to the vessel wall
*1: Ikari Y, Nagaoka M, Kim JY, Merino Y, Tanabe T. The physics of guiding catheters for the left coronary artery in transfemoral and trans-radial interventions. J Invasive Cardio. 2005 Dec; 17(12): 636-641.*2: Youssef AA, Hsieh YK, Cheng CI, We CJ. A single trans-radial guiding catheter for right and left coronary angiography and intervention. Euro intervention 2007; 3: 475-481.
Patients who have had cardiac catheterization or coronary angioplasty often are required to stay in bed with restricted movement for three to 24 hours afterward to prevent bleeding from the femoral artery catheter insertion site.
Features and Benefits
Improved back up support in comparison to Terumo standard femoral guiding catheter shapes*1
*1: Based on comparative studies made among Terumo Guiding Catheters*2: Ekari Y, Nagaoka M, Kim JY, Merino Y, Tanabe T. The physics of guiding catheters for the left coronary artery in transfemoral and trans-radial interventions. J Invasive Cardio. 2005 Dec; 17(12): 636-641.*3: Youssef AA, Hsieh YK, Cheng CI, We CJ. A single trans-radial guiding catheter for right and left coronary angiography and intervention. Euro intervention 2007; 3: 475-481.
Guide catheters are required for all coronary interventions to provide access to the coronary ostium and support equipment delivery. The ideal guide provides stability for device advancement through the coronary anatomy, while minimizing vessel trauma and allowing for vessel opacification.
The catheter is guided to the narrowed artery. Then, a smaller balloon catheter is inserted through the flexible catheter and inflated at the narrowed area to open it. Often, the doctor will also place a mesh coil called a stent at the narrowed part to help keep the artery open.
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