DESIGNED BY PERFUSIONISTS. ENGINEERED BY MEDTRONIC.
The Affinity Fusion™ oxygenation system’s design is based on input from more than 500 perfusionists worldwide. Thoughtfully engineered from inlet to outlet, the Affinity Fusion™ oxygenation system takes a fundamentally different design approach:
Proactive air handling
Haemocompatibility
Improved flexibility
Integrated arterial filter
Expanded heat exchanger and gas transfer capabilities
PRODUCT DETAILS: AFFINITY FUSION™ OXYGENATION SYSTEM
Both oxygenator and reservoir device have:
Blood-contacting materials made from BPA* – and DEHP-free polymers
The higher density structure of the Affinity Fusion™ polyethylene terephthalate (PET) heat exchanger provides improved chemical resistance with a low permeability factor when compared to lower density plastics such as polyurethane or TPU*.
PET heat exchanger features and benefits:
Resistant to chemical migration
Durable to withstand the surrounding environment
Small tube design of capillaries increases heat exchange performance
Decreases prime volume
Enables device incineration
Oxygenator Features
Cardiotomy/Venous Reservoir Features
Integrated arterial filter
25 µm filtration
260 mL prime
Enhanced gas transfer
Plastic heat exchanger (PET)
Recirculation and cardioplegia ports
½” quick-connect water ports
Ambidextrous design
BPA-free plastic
Clear housing
Volume-displacing leur caps
Built-in temp probe sleeve
1-7 L/min flow
Balance™ biosurface
Cortiva™ BioActive surface
4500 mL capacity
360-degree rotating venous inlet
Curved venous inlet with 2 angled luer ports
Built-in temperature probe sleeve
360-degree rotating cardiotomy inlet with 4 luer ports
2 nonfiltered luer ports
Antifoam in venous and cardiotomy filters
Pressure relief valve
VAVD ready
BPA-free plastic*
Removable sampling manifold
Clear housing
1-7 L/min flow
200 mL @7 L/min minimum operating level
Balance™ biosurface
AFFINITY FUSION™ OXYGENATION SYSTEM SPECIFICATIONS
OXYGENATOR
Membrane type
Microporous polypropylene hollow fiber
Membrane surface area
2.5m2
Heat exchange surface material
Polyethylene terephthalate (PET)
Static priming volume
260 mL
Recommended blood flow rate
1-7 L/min
Maximum water side pressure
30 psi
Maximum blood pressure
750 mm Hg
Arterial outlet port
3/8″
Venous inlet port
3/8″
Arterial sample port
Female luer port
Recirculation port
1/4″
Cardioplegia port
1/4″
Gas inlet port
1/4″ nonbarbed
Gas outlet port
3/8″ nonbarbed
Water ports
1/2″ quick disconnects
Filtration
25 µm
CARDIOTOMY/VENOUS RESERVOIR
Reservoir volume capacity
4500 ml
Recommended blood flow rate
1-7 L/min
Maximum cardiotomy flow rate
6 L/min
Minimum operating level
200 mL at 7L/min
Cardiotomy filtration
30 µm
Venous screen
105 µm
Venous inlet, rotatable
1/2″ with 3/8″ adapter
Venous reservoir outlet
3/8″
Vent/VAVD port
1/4″ nonbarbed
Cardiotomy port (4)
1/4″
Cardiotomy port (1)
3/8″
Prime port
1/4″ nonbarbed
Recirculation port
1/4″
Filtered luer lock ports
4
Non-filtered luer lock ports
2
Venous luer lock ports
2
Positive pressure relief valve crack
<5 mm Hg
Vacuum pressure relief valve crack
100 mm Hg average
ORDERING INFORMATION
Affinity Fusion™ Oxygenation Systems
Model#
Product Description
Units/case
CB841
Oxygenator with integrated arterial filter with Cortiva bioactive surface and cardiotomy/venous reservoir with Balance biosurface
1
BB841
Oxygenator with integrated arterial filter and cardiotomy/venous reservoir with Balance biosurface
1
CB811
Oxygenator with integrated arterial filter and Cortiva bioactive surface
1
BB811
Oxygenator with integrated arterial filter and Balance biosurface
1
Affinity Fusion™ Accessories and Holders
Model #
Product Description
Units/Case
AUH2093
Affinity™ orbit holder system
1
ATP210
Temperature probe
1
AMH2014
Affinity™ manifold holder
1
RCL841
Recirculation line
12
MANUALS AND TECHNICAL GUIDES
Instructions for Use
Find this technical manual in the product labeling supplied with each device.
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.
Designed with continuous broad-spectrum antimicrobial activity in the drape adhesive where it can’t be washed away
Clinically shown to help reduce the risk of wound contamination and immobilize bacteria on the skin1,2
Complies with NICE guidance on the use of incise drapes. Ioban is an iodophor impregnated drape with clinical evidence to support its performance.
Specifications
Brands
Ioban™
Cladimed Code
E51BA99
Features
Antimicrobial
Incise Area Length (metric)
56 cm
Incise Area Width (metric)
45 cm
Material
Fabric
Overall Length (Metric)
66 cm
Overall Width (Metric)
45 cm
Procedure
General Surgery
Product Type
Incise Drapes
Product Type Free Format
Antimicrobial Incise Drape
Product Use
Incise
Units per Pack
10
Details
Highlights
Designed with continuous broad-spectrum antimicrobial activity in the drape adhesive where it can’t be washed away
Clinically shown to help reduce the risk of wound contamination and immobilize bacteria on the skin1,2
Complies with NICE guidance on the use of incise drapes. Ioban is an iodophor impregnated drape with clinical evidence to support its performance
High moisture-vapour transmission rate (MVTR) for breathability ensuring adhesion throughout the procedure
Low memory stretch allows limb mobilisation or heavy retraction with reduced tension to the skin
References 1. Dewan PA, Van Rij AM, Robinson RG, Skeggs GB, Fergus M. The use of an iodophor impregnated plastic incise drape in abdominal surgery – a controlled clinical trial. 2. French MLV, Eitzen HE, Ritter MA. The plastic surgical adhesive drape: an evaluation of its efficacy as a microbial barrier. 3. Bejko J, Tarsia V, Carrozzini M, et al. Comparison of efficacy and cost of iodine impregnated drape vs. standard drape in cardiac surgery: study in 5100 patients. 4. Rezapoor M, Tan TL, Maltenfort MG, Parvizi J. Incise draping reduces the rate of contamination of the surgical site during hip surgery: a prospective, randomized trial. 5. Alexander JW, Aerni S, Plettner JP. Development of a safe and effective one minue preoperative skin preparation
3M™ Ioban™ 2 Antimicrobial Incise Drapes effectively help prevent wound contamination. Evidence shows that applying an antimicrobial incise drape is a critical step in reducing the risk of wound contamination that may be associated with Surgical Site Infection (SSI).3,4 Antimicrobial Incise Drape Incise area 60cm x 45cm
Micro organisms from the patient’s skin are the most common cause of surgical site infection (SSI). Ioban 2 antimicrobial incise drapes help to reduce the risk of SSI by immobilising micro organisms and delivering antimicrobial activity at the skin surface and deeper layers.
Cross IT 200 XT Guide Wire is intended to facilitate the placement of balloon dilatation catheters during percutaneous transluminal coronary angioplasty (PTCA) and percutaneous transluminal angioplasty (pta).
GRAFTMASTER RX is indicated for use in the treatment of free perforations, defined as free contrast extravasation into the pericardium, in native coronary vessels or saphenous vein bypass grafts ≥ 2.75 mm in diameter. The effectiveness of this device for this use has not been demonstrated. You
The HI-TORQUE PILOT 50 guide wires are polymer-tipped wires with a lubricious, hydrophilic coating. These wires provide excellent distal access with superb torque transmission and variable tip stiffness
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:
402-03
Weight:
3.00 LBS
Availability:
2-3 Business days
Shipping:
Calculated at checkout
Quantity:
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 50
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
BLOOD DIAGNOSTICS AND CLOT DETECTION In addition to running cardiopulmonary bypass, we know that you rely on accurate blood diagnostic results.
The ACT Plus® System combines a trusted standard in precise clot detection technology with state-of-the-art user features including data management and connectivity-ready capabilities. It is a microprocessor-controlled electromechanical coagulation instrument designed to determine coagulation endpoints in fresh and citrated whole blood samples. Clotting-time results are presented on the instrument’s Clot Time Display (CTD) and Liquid Crystal Display (LCD) screens.
The ACT Plus System provides long-term data storage and retrieval, with access to previous patient and quality control test data. Test results are stored in the order in which they are performed. The ability to externally transfer or save data enhances the system’s versatility.
The ACT Plus System is portable and well suited for all point-of-care testing situations. It offers the reliability required in:
Cardiovascular and vascular surgery ECMO Cardiac catheterization laboratories Critical care units Hemodialysis units MANAGE YOUR ACT PLUS SYSTEM DATA EFFICIENTLY AND EFFECTIVELY As part of our ongoing commitment to helping you manage your work efficiently and effectively, we offer the ACT Plus EDM external data manager to accompany the ACT Plus Automated Coagulation Timer System.
By combining this powerful software with the ACT Plus System, you will have access to the reports you’ll need to analyze test results and make informed decisions. This timesaving data management solution offers added convenience, reassurance and confidence—allowing you to stay focused on improving patient outcomes.
The ACT Plus EDM is a versatile Microsoft Access-based data management software application that runs on a PC and is designed to help you manage your patient, QC, instrument and user ID data. All aspects of Microsoft Access software required to run the application are included with the ACT Plus EDM.
ACT Plus Instrument
Order Number
Description
# of Units
ACT100
ACT Plus System is a microprocessor-controlled electromechanical coagulation instrument for determination of activated coagulation times
1 per box
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
ACT® CLOTtrac® Coagulation Controls
550-01
CLOTtrac CWB Coagulation Control – Verify performance of 402-01 and 402-02 cartridges, and the ACT Plus Instrument (when performing QC on the LR ACT cartridge (#402-01), calcium chloride (#550-11) must be added with the CLOTtrac CWB coagulation control)
15 per box
550-07
CLOTtrac HR Coagulation Control – Verify performance of 402-03, and 402-07 cartridges and the ACT Plus Instrument
15 per box
550-08
CLOTtrac HR Abnormal Coagulation Control – Verify performance of 402-03 cartridges and the ACT Plus Instrument
15 per box
550-09
CLOTtrac LR Abnormal Coagulation Control – Verify performance of 402-01 cartridges and the ACT Plus® Instrument (when performing QC on the LR ACT cartridge (#402-01), calcium chloride (#550-11) must be added with the CLOTtrac LR abnormal coagulation control)
15 per box
550-10
CLOTtrac RACT Abnormal Coagulation Control – Verify performance of 402-02 cartridges and the ACT Plus® Instrument
15 per box
550-12
CLOTtrac HTC Coagulation Control – Verify performance of 402-07 cartridges and the ACT Plus® Instrument
15 per box
550-13
CLOTtrac HR Control Pack – Verify performance of 402-03 cartridges and the ACT Plus Instrument (contains 15 HR Normal and 15 HR Abnormal)
15 per box
550-11
Calcium Chloride 5 ml vial – Use with control nos. 550-01, 550-09 in cartridge 402-01
A PROM test proven to be accurate even in patients with variable amounts of vaginal bleeding. Other point-of-care PROM tests are only indicated for use with trace vaginal bleeding while Actim PROM has been proven to perform with more than trace amounts of vaginal bleeding1. With up to 20% of women presenting with vaginal bleeding at the time of PROM diagnosis2, you need a reliable test for all patients. The Actim PROM advantages are clear:
Multiple clinical studies have proven Actim PROM’s accuracy in the presence of blood
20 years of proven results outside the U.S. with more than 5,000,000 PROM tests performed
Fastest POC test available, with accurate results within 5 minutes
1 The test has been designed to minimize interference from bleeding, but in cases of heavy bleeding the blood locally may have a higher concentration of IGFBP-1 protein. In these cases, a positive result should be interpreted with caution. Actim PROM Instructions for Use
2 Palacio et al.: Meta-analysis of studies on biochemical marker tests for the diagnosis of premature rupture of membranes: comparison of performance indexes. BMC Pregnancy and Childbirth 2014 14:183
A PROM test proven to be accurate even in patients with variable amounts of vaginal bleeding. Other point-of-care PROM tests are only indicated for use with trace vaginal bleeding while Actim PROM has been proven to perform with more than trace amounts of vaginal bleeding1. With up to 20% of women presenting with vaginal bleeding at the time of PROM diagnosis2, you need a reliable test for all patients. The Actim PROM advantages are clear:
Multiple clinical studies have proven Actim PROM’s accuracy in the presence of blood
20 years of proven results outside the U.S. with more than 5,000,000 PROM tests performed
Fastest POC test available, with accurate results within 5 minutes
1 The test has been designed to minimize interference from bleeding, but in cases of heavy bleeding the blood locally may have a higher concentration of IGFBP-1 protein. In these cases, a positive result should be interpreted with caution. Actim PROM Instructions for Use
2 Palacio et al.: Meta-analysis of studies on biochemical marker tests for the diagnosis of premature rupture of membranes: comparison of performance indexes. BMC Pregnancy and Childbirth 2014 14:183
An alternative to the articulating RUMI II, the reusable Advincula Arch is ideal for physicians who prefer the simple and lightweight design of a disposable uterine manipulator but would like additional strength. Some physicians choose the Advincula Arch because they prefer executing anteversion/retroversion of the uterus manually. The radial design permits easy insertion from any angle and its unique curve provides outstanding elevation for superior visualization and control. See related products below.
Provides: • Ease of use • Functionality for a faster, safer TLH An alternative to the articulating RUMI
II, the reusable Advincula Arch™ is ideal for physicians who prefer the simple and lightweight design of a disposable uterine manipulator but would like additional strength. Some physicians choose the Advincula Arch™ as they prefer executing anteversion/retroversion of the uterus manually or with the Uterine Positioning System™. The radial design permits easy insertion from any angle and its unique curve provides outstanding elevation for superior visualization and control. The Advincula Arch™ has a specifically designed Koh-Efficient ™ system enabling the physician to safely insert and correctly position the device for use.
Exceptional strength and performance in an easy-to-use disposable uterine manipulator. The Advincula Delineator™ is designed for TLH, LSH and LAVH procedures.
Koh-Efficient system is integrated into the Delineator.
Rigid Koh Colpotomy cup clearly delineates the vaginal fornices with proper cephalad pressure.
Ergonomic handle fits comfortably in your hand through the entire procedure.
Parts & Accessories
AD750-KE25
Advincula Delineator 2.5CM Ultem Plastic Cup (3 per box) for use with electrosurgical devices
AD750-KE30
Advincula Delineator 3.0CM Ultem Plastic cup (3 per box) for use with electrosurgical devices
AD750-KE35
Advincula Delineator 3.5CM Ultem Plastic cup (3 per box) for use with electrosurgical devices
AD750-KE40
Advincula Delineator 4.0CM Ultem Plastic cup (3 per box) for use with electrosurgical devices
AD750-KES25
Advincula Delineator 2.5CM stainless steel cup (3 per box) for use with harmonic scalpel and laser devices
AD750-KES30
Advincula Delineator 3.0CM stainless steel cup (3 per box) for use with harmonic scalpel and laser devices
AD750-KES35
Advincula Delineator 3.5CM stainless steel cup (3 per box) for use with harmonic scalpel and laser devices
AD750-KES40
Advincula Delineator 4.0CM stainless steel cup (3 per box) for use with harmonic scalpel and laser devices
AD750SC-KE25
Advincula Delineator 2.5CM Plastic Cup (3 per box) flexible soft cup
AD750SC-KE30
Advincula Delineator 3.0CM Plastic Cup (3 per box) flexible soft cup
AD750SC-KE35
Advincula Delineator 3.5CM Plastic Cup (3 per box) flexible soft cup
AD750SC-KE40
Advincula Delineator 4.0CM Plastic Cup (3 per box) flexible soft cup
The device creates a mechanical seal by sandwiching the arteriotomy between a bioabsorbable anchor and collagen sponge, which dissolve in 60 to 90 days.
Three bioabsorbable components actively seal the arteriotomy:
Anchor: Bioabsorbable co-polymer anchor placed against the inside of the vessel wall
Collagen: Placed on top of the arteriotomy in the tissue tract
Suture: Cinches the anchor and collagen together to form a secure seal.
LOCATE THE ARTERY
Exchange the procedure sheath with the Angio-Seal locator system.
Blood flow through the locator visually confirms proper sheath position in the artery.
SET THE ANCHOR
Insert the Angio-Seal VIP device into the sheath until you hear a “click.”
Gently pull back on the locking cap until you hear another “click.”
The anchor is now locked in place and device is ready to be deployed.
SEAL THE PUNCTURE
Gently pull back on the Angio-Seal VIP device until the suture has stopped spooling.
Maintain upward tension on the device and gently advance the compaction tube until resistance is felt.
Cut the suture and remove the device.
ANGIO-SEAL VIP PRODUCT CODES
Part Number
French Size
Guidewire Diameter (in)
610130
6Fr
.035 Wire
610131
8Fr
.038 Wire
REFERENCES
RX ONLY. Refer to the product labels and package insert for complete warnings, precautions, potential complications, and instructions for use.
Nash JE, Evans DG. (1999). The Angio‐Seal hemostatic puncture closure device. Concept and experimental results. Herz, 24(8), 597‐606.
Per Instructions For Use ASIN0004 revision 2018-09-01.
Indications: The Angio-Seal Vascular Closure Device product family, including the VIP and Evolution platforms, is indicated for use in closing and reducing time to hemostasis of the femoral arterial puncture site in patients who have undergone diagnostic angiography procedures or interventional procedures using an 8 French or smaller procedural sheath for the 8 F Angio-Seal device and a 6 French or smaller procedural sheath for the 6 F Angio-Seal device. The Angio-Seal VIP and Evolution platform devices are also indicated for use to allow patients who have undergone diagnostic angiography to safely ambulate as soon as possible after sheath removal and device placement, as well as to allow patients who have undergone an interventional procedure to safely ambulate after sheath removal and device placement.
Important Safety Information:
Possible adverse events for vascular closure devices include, but are not limited to: bleeding or hematoma, AV fistula or pseudoaneurysm, infection, allergic reaction, foreign body reaction, inflammation or edema. This device should only be used by a licensed physician (or other health care professional authorized by or under the direction of such physician) possessing adequate instruction in the use of the device, e.g., participation in an Angio-Seal physician instruction program or equivalent.
AngioSculpt RX PTCA scoring balloon catheter significantly alters the landscape for treating CAD, offering the advanced performance that only an innovative clinical solution can provide. The AngioSculpt RX PTCA scoring balloon catheter is the only specialty scoring device indicated for ISR and complex type-C lesions.
Features
Advanced molded, tapered tip
New tip designed for improved delivery.
Power: ~15 – 25x scoring force
AngioSculpt RX PTCA has an enhanced mechanical advantage. The leading edges are designed to drive outward expansion with up to 15–25 times the force of conventional balloons.² The helical nitinol scoring element creates a large luminal expansion for stent implantation.³
Precision: Edges locked in
Achieve proper placement as AngioSculpt’s rectangular scoring edges lock the device in place. AngioSculpt has minimal device slippage or “watermelon seeding,” even in ISR.¹
Safety: ~1x force post-scoring
Get predictable results with AngioSculpt RX PTCA. Post-scoring, outward forces are designed to be equivalent to that of a conventional balloon. AngioSculpt RX PTCA has a low dissection rate of 13.6% (majority were non-flow limiting).¹
• Sharp, dual cutting edge for clean, precise removal of aortic tissue • Conical tip for easy insertion by straight or button-hole technique • Two handle lengths for better control and maneuverability • Sterile and disposable for efficiency and patient safety • Ten blade sizes for trimming to desired size and shape: 2.5-6.0 mm
ORDERING INFORMATION
Diameter Order # Order # (mm) Standard Handle Long Handle 2.5 APU425 APU525 3.0 APU430 APU530 3.5 APU435 APU535 4.0 APU440 APU540 4.4 APU444 APU544 4.8 APU448 APU548 5.0 APU450 APU550 5.2 APU452 APU552 5.6 APU456 APU556 6.0 APU460 APU560
Intended Use
Medtronic Aortic Punches are intended for use by cardiac surgeons during coronary artery bypass grafting procedures to create an opening in the wall of the vessel. Each punch is for single-patient use only. Resterilization is not recommended.
Supply
Medtronic Aortic Punches are supplied sterile in individual blister packs, six packs of the same size per box. Caution: Federal law (USA) restricts this device to sale by or on the order of a physician. For a listing of indications, contraindications, precautions and warnings, please refer to the Directions For Use.
n an endeavour to give our clients customized range of Arthroscopic Punch, we work as per their specific requirements. Our offered Arthroscopic Punch t is perfectly stitched and gives ease to the user. Our products ranges are manufactured using the supreme quality of raw material in compliance with the set industrial norms.
Smoothbore products provide low resistance to flow while external coil reduces kinks & blockages.
Extendable product provides a lightweight and flexible solution
Double swivel connector increases ease of use
Double cap to maintain PEEP during suctioning or bronchoscopy – Each catheter mount and airway connector is equipped with a red safety cap so that the system is completely closed and protected until directly prior to use on the patient
22F/15M connector on device side as a two-in-one solution
Standardized connectors for safe connection to other components
Luer-Lock port for gas sampling
Disposable convenience enhances workflow
PVC-free design of gas leading components eliminates risk of softeners such as DEHP
Precision engineering ensures unmatched performance in tortuous anatomy
LOW PROFILE MICROCATHETER
Excellent crossing profile: 1.9Fr (0.62mm)
Low profile design to cross microchannels
2 Caravels fit in a 6Fr guide catheter
INTERNAL LUMEN INTEGRITY
Enhanced resistance to kinking in tortuous anatomy
Facilitates optimal guide wire performance
ACT ONE Maintains Inner Lumen:
Ordering Information
OUTER DIAMETER (FR(MM))
INNER DIAMETER (INCH(MM))
PRODUCT
CATALOG NO.
TIP
DISTAL SHAFT
PROXIMAL SHAFT
TIP
SHAFT
USABLE LENGTH (CM)
HYDROPHILIC COATING LENGTH (CM)
ASAHI Caravel, 135cm
CRV135-19P
1.4 (0.48)
1.9 (0.62)
2.6 (0.85)
0.016 (0.40)
0.022 (0.55)
135
70
ASAHI Caravel, 150cm
CRV150-19P
1.4 (0.48)
1.9 (0.62)
2.6 (0.85)
0.016 (0.40)
0.022 (0.55)
150
85
Indications for Use
This microcatheter is intended to provide support to facilitate the placement of guide wires in the coronary and peripheral vasculatures, and can be used to exchange one guide wire for another. This microcatheter is also intended to assist in the delivery of contrast media into the coronary and peripheral vasculatures. Do not use this microcatheter other than for use in the coronary and peripheral vasculatures.
Designed to add 165cm to the end of an ASAHI non-300cm wire
TIP SHAPE
Ordering Information
PRODUCT
CATALOG NO.
TIP SHAPE
LENGTH (CM)
ASAHI EXTENSION 165
AG149001
Straight
165
Indications for Use
ASAHI PTCA Guide Wires are intended to facilitate the placement of balloon dilation catheters during percutaneous transluminal coronary angioplasty (PTCA) and percutaneous transluminal angioplasty (PTA). The ASAHI PTCA Guide Wires are not to be used in the neurovasculature.
Standard wire of tapered, low tip load, polymer jacket guide wire for channel crossing and loose tissue tracking.
■Fielder XT-A
Tip load 1.0gf guide wire.
Torque and control enhance crossability for the occluded lesions without a stump.
■Fielder XT-R
Tip load 0.6 gf guide wire.
Flexibility and control provide trackability for the channel tracking and sub total occlusion (99%).
■Trackability
Flexibility & control provide trackability
XT-R had better performance for the channel tracking
■Torque Response
It provides better control ability by fixing guide wire tip to the right direction.
■Small tip shapeability
It provides the potential for the loose tissue and collateral channel tracking by a small curve and tapered tip.
* All the data were obtained by company standardized test, which may differ from industry standardized tests.
* All the data do not prove that all devices have exactly the same performance with the samples used for these tests.
Good choice guide wire when extra support for delivery of interventional devices is required.
TIP LOAD
TIP RADIOPACITY
4 cm
COATING
HYDROPHOBIC (SILICONE)
Hydrophobic coating over spring coil
TIP SHAPE
Ordering Information
PRODUCT
CATALOG NO.
TIP SHAPE
LENGTH (CM)
DIAMETER (INCH(MM))
RADIOPAQUE SEGMENT (CM)
SPRING COIL LENGTH (CM)
COATING
GRAND SLAM 180 cm, Straight
AG141002
Straight
180
0.014 (0.36)
4
4
HYDROPHOBIC (SILICONE)
Hydrophobic coating over spring coil
GRAND SLAM 180 cm, J Shape
AG141002J
J Shape
180
0.014 (0.36)
4
4
HYDROPHOBIC (SILICONE)
Hydrophobic coating over spring coil
GRAND SLAM 300 cm, Straight
AG141302
Straight
300
0.014 (0.36)
4
4
HYDROPHOBIC (SILICONE)
Hydrophobic coating over spring coil
GRAND SLAM 300 cm, J Shape
AG141302J
J Shape
300
0.014 (0.36)
4
4
HYDROPHOBIC (SILICONE)
Hydrophobic coating over spring coil
Indications for Use
ASAHI PTCA Guide Wires are intended to facilitate the placement of balloon dilation catheters during percutaneous transluminal coronary angioplasty (PTCA) and percutaneous transluminal angioplasty (PTA). The ASAHI PTCA Guide Wires are not to be used in the neurovasculature.
Hydrophobic guide wire for choronic occlusion cases. The core wire and distal coil are designed to resist great force thus lowering the chances of getting trapped in a lesion
A workhorse frontline guide wire with ACT ONE construction for torque response and increased durability. Also has a polymer jacket for lubricity. High tip flexibility improves trackability in tortuous anatomy.
TIP LOAD
TIP RADIOPACITY
3 cm
COATING
HYDROPHILIC* coating on a polymer jacket and core wire
TIP SHAPE
Ordering Information
PRODUCT
CATALOG NO.
TIP SHAPE
LENGTH (CM)
DIAMETER (INCH(MM))
RADIOPAQUE SEGMENT (CM)
SPRING COIL LENGTH (CM)
COATING
ASAHI SION black 190cm, Straight
APW14R010S
Straight
190
0.014 (0.36)
3
12
Polymer Jacket & Hydrophilic*
ASAHI SION black 190cm, J Shape
APW14R010J
J Shape
190
0.014 (0.36)
3
12
Polymer Jacket & Hydrophilic*
ASAHI SION black 190cm, Pre-Shape
APW14R010P
Pre-Shape
190
0.014 (0.36)
3
12
Polymer Jacket & Hydrophilic*
ASAHI SION black 300cm, Straight
APW14R310S
Straight
300
0.014 (0.36)
3
12
Polymer Jacket & Hydrophilic*
ASAHI SION black 300cm, J Shape
APW14R310J
J Shape
300
0.014 (0.36)
3
12
Polymer Jacket & Hydrophilic*
ASAHI SION black 300cm, Pre-Shape
APW14R310P
Pre-Shape
300
0.014 (0.36)
3
12
Polymer Jacket & Hydrophilic*
Indications for Use
ASAHI PTCA Guide Wires are intended to facilitate the placement of balloon dilation catheters during percutaneous transluminal coronary angioplasty (PTCA) and percutaneous transluminal angioplasty (PTA). The ASAHI PTCA Guide Wires are not to be used in the neurovasculature.
Extra support front line guide wire that stabilizes the guide catheter for stress-free device delivery
“While providing much higher support for device delivery, SION blue ES shows great steerability found in SION family guide wires.
■Steerability
・Composite core and balanced core wire design provides great steerability and maneuverability. Usable as a frontline guide wire with easy control for branch selection and minimal loss of steerabilityin tortuous vessels.
■Device delivery
– Helps provide back-up support to the guide catheter – Less stress during the procedure due to guiding catheter stabilization – Easy device tracking due to vessel straightening
■Tip flexibility
The distal 5cm has the flexibility of the SION series.
■SION series positioning
* All the data were obtained by company standardized test, which may differ from industry standardized tests.
Frontline guide wire with proprietary ACT ONE construction for greater tip flexibility, durability and torque response.
(Easily-discernible shaft color for differentiation from other ASAHI wires.)
TIP LOAD
TIP RADIOPACITY
3 cm
COATING
HYBRID COATING: HYDROPHILIC* WITH HYDROPHOBIC TIP
Hydrophobic Coating: Tip to 1.5 cm
Hydrophilic Coating: 18.5 cm
TIP SHAPE
Resources
Guide wire differences between Torque and no Torque
Traversing a tortuous vessel, whether for Interventional Cardiology or Interventional Neurology can require a guide wire that is an extended version of the Interventional Cardiologist or Neurologist own finger. To achieve this, torque technology, like ASAHI’s own patented guide wires, is needed for accurate pushback and little to no whip. See a firsthand example of a guide wire with and without this torque ability.
Crossing the Y-Branch
A side branch occlusion? a tortuous vessel? Not a problem with the right ASAHI INTECC guide wire technology. See it for yourself!
ASAHI PTCA Guide Wires are intended to facilitate the placement of balloon dilation catheters during percutaneous transluminal coronary angioplasty (PTCA) and percutaneous transluminal angioplasty (PTA). The ASAHI PTCA Guide Wires are not to be used in the neurovasculature.
Good choice for septal navigation/surfing. Flexible tip and ultra low tipload improve navigation in angulated and tortuous collaterals (do not torque).
Flexible tip and shaft provide superb trackability and crossability in severe tortuosity.
TIP LOAD
TIP RADIOPACITY
3 cm
COATING
HYDROPHILIC*
Hydrophilic coating: 52 cm
TIP SHAPE
Ordering Information
PRODUCT
CATALOG NO.
TIP SHAPE
LENGTH (CM)
DIAMETER (INCH(MM))
RADIOPAQUE SEGMENT (CM)
SPRING COIL LENGTH (CM)
COATING
ASAHI SUOH 03 190cm, Straight
AHW14R013S
Straight
190
0.014 (0.36)
3
19
HYDROPHILIC*
Hydrophilic coating: 52 cm
ASAHI SUOH 03 190cm, Pre-shape
AHW14R013P
Pre-shape
190
0.014 (0.36)
3
19
HYDROPHILIC*
Hydrophilic coating: 52 cm
ASAHI SUOH 03 300cm, Straight
AHW14R313S
Straight
300
0.014 (0.36)
3
19
HYDROPHILIC*
ASAHI SUOH 03 300cm, Pre-shape
AHW14R313P
Pre-shape
300
0.014 (0.36)
3
19
HYDROPHILIC*
Indications for Use
ASAHI PTCA Guide Wires are intended to facilitate the placement of balloon dilation catheters during percutaneous transluminal coronary angioplasty (PTCA) and percutaneous transluminal angioplasty (PTA). The ASAHI PTCA Guide Wires are not to be used in the neurovasculature.
Ordering Information
