PROGREAT® MICROCATHETHER
PRODUCT OVERVIEW
PROGREAT® Microcatheters are designed to allow navigation through tortuous peripheral vessels for optimal access and delivery of therapeutic embolization.
Terumo Progreat 2.7Fr. Microcatheter is Designed to provide optimal trackability and support even in the most tortuous anatomy.
DESIGNED TO CONFIDENTLY DELIVER EMBOLOTHERAPY
- Tungsten coil reinforcement for kink resistance2
- PTFE inner layer is designed for exceptional guidewire tracking, with virtually frictionless delivery of coils and other embolics2
- DMSO Compatible3
- Radiopaque 0.7 mm platinum/iridium markers allow for rapid and precise positioning4

DESIGNED TO ENHANCE ACCESS TO SMALL PERIPHERAL VESSELS
- TERUMO Glide TechnologyTM hydrophilic coating enhances navigation through tortuous anatomy1,2
- Unique varied tungsten coil pitch construction provides distal flexibility and proximal pushability, enhancing vessel selectivity and catheter placement.

PROGREAT® COAXIAL MICROCATHETER SYSTEM
- Preloaded with uniquely designed 0.021” GLIDEWIRE® GT for the 2.8Fr system and 0.018″ GLIDEWIRE® GT for the 2.4Fr system1
- Available in 2.8Fr and 2.4Fr
- Enables simultaneous preparation of microcatheter and guidewire, which may save time and increase procedural efficiency1
PROGREAT 2.4 COAXIAL PROVEN TO REACH DISTAL VESSELS WITH EASE⁴
- Provides greater vessel selectivity and demonstrated superiority in traversing tortuous anatomy
- Provides best-in-class kink resistance, demonstrated in both the distal and proximal shaft.

PROGREAT® Microcatheter Product Codes
Includes hemostatic valve and shaping mandrel
| Fr Size | Product Code | Length (cm) | Tip Shape | Max Pressure (psi) | RO Markers | Hydrophilic Coating Length (cm) |
| 2.4 | MC*PB2411Y | 110 | Straight | 750 | 1 | 50 |
| MC*PB2413Y | 130 | Straight | 1 | 70 | ||
| MC*PB2413ZRA | 130 | 70 Deg. Angle | 1 | 70 | ||
| MC*PB2413ZRC | 130 | J Curve | 1 | 70 | ||
| MC*PV2415Y | 150 | Straight | 2 | 90 | ||
| MC*PV2415ZRA | 150 | 70 Deg. Angle | 2 | 90 | ||
| MC*PV2415ZRC | 150 | J Curve | 2 | 90 | ||
| 2.7 | MC*PC2711Y | 110 | Straight | 750 | – | 50 |
| MC*PC27137 | 130 | Straight | – | 70 | ||
| 2.8 | MC*PB2811Y | 110 | Straight | 900 | 1 | 50 |
| MC*PB2813Y | 130 | Straight | 1 | 70 | ||
| MC*PV2815Y | 150 | Straight | 2 | 90 |
PROGREAT® Coaxial Microcatheter System Codes
Includes unique GLIDEWIRE® GT Guidewire, wire stopper, guidewire introducer, hemostatic valve, 2.5 mL syringe, and shaping mandrel
| Fr Size | Product Code |
Length (cm) |
Max Pressure (PSI) |
RO Markers | Hydrophilic Coating Length (cm) |
Glidewire® GT Length (cm) |
Glidewire® GT Size (in) |
| 2.4 Fr | MC*PE24111YB | 110 | 750 | 1 | 50 | 120 | 0.018 |
| 2.4 Fr | MC*PE24131YB | 130 | 750 | 1 | 70 | 140 | 0.018 |
| 2.4 Fr | MC*PE24151YV | 150 | 750 | 2 | 90 | 160 | 0.018 |
| 2.7 Fr | MC*PE27111Y | 110 | 750 | – | 50 | 120 | 0.021 |
| 2.7 Fr | MC*PE27131Y | 130 | 750 | – | 70 | 140 | 0.021 |
| 2.8 Fr | MC*PE28111YB | 110 | 900 | 1 | 50 | 120 | 0.021 |
| 2.8 Fr | MC*PE28131YB | 130 | 900 | 1 | 70 | 140 | 0.021 |
| 2.8 Fr | MC*PE28151YV | 150 | 900 | 2 | 90 | 160 | 0.021 |
PRODUCT SPECIFICATIONS
| Catheter OD | Length (cm) |
Inner Diameter (in/mm) |
Max GW (in) |
Embolic Compatibility |
Dead Space Volume (mL) |
Actual Flow Rate* (mL/sec) @ 750 psi | Actual Flow Rate* (mL/sec) @ 900 psi |
| 2.4/2.9Fr (0.80/0.97mm) |
110 | 0.022″/0.57 | 0.018″ | 0.018″ Coils/HydroPearl® 600 ± 75 μm |
0.48 | 2.3 | – |
| 2.4/2.9Fr (0.80/0.97mm) |
130 | 0.022″/0.57 | 0.018″ | 0.018″ Coils/HydroPearl® 600 ± 75 μm |
0.53 | 2 | – |
| 2.4/2.9Fr (0.80/0.97mm) |
150 | 0.022″/0.57 | 0.018″ | 0.018″ Coils/HydroPearl® 600 ± 75 μm |
0.58 | 1.8 | – |
| 2.7/2.9Fr (0.90/0.97mm) |
110 | 0.025″/0.065 | 0.021″ | 0.018″ Coils/HydroPearl® 800 ± 75 μm |
0.57 | 3.5 | – |
| 2.7/2.9Fr (0.90/0.97mm) |
130 | 0.025″/0.065 | 0.021″ | 0.018″ Coils/HydroPearl® 800 ± 75 μm |
0.64 | 3.2 | – |
| 2.8/3.0Fr (0.93/1.00mm) |
110 | 0.027″/0.70 | 0.021″ | 0.018″ Coils/HydroPearl® 800 ± 75 μm |
0.61 | 4.1 | 4.7 |
| 2.8/3.0Fr (0.93/1.00mm) |
130 | 0.027″/0.70 | 0.021″ | 0.018″ Coils/HydroPearl® 800 ± 75 μm |
0.68 | 3.7 | 4.3 |
| 2.8/3.0Fr (0.93/1.00mm) |
150 | 0.027″/0.70 | 0.021″ | 0.018″ Coils/HydroPearl® 800 ± 75 μm |
0.75 | 3.1 | 3.9 |
REFERENCES
RX ONLY. Refer to the product labels and package insert for complete warnings, precautions, potential complications, and instructions for use.
- Catheter [Instructions for Use]. Somerset, NJ: Terumo Medical Corporation; 2016
- PROGREAT Catheter 510(k); 2003
- PROGREAT DMSO Compatibility Statement Letter
- Data on file.
PROGREAT® MICROCATHETHER
2 reviews for PROGREAT® MICROCATHETHER
Related products
-
CLOSUREFAST
ClosureFast™
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
- 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.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
-
NC EUPHORA NONCOMPLIANT BALLOON CATHETER
NC Euphora™ noncompliant balloon
NC Euphora™ noncompliant balloon dilatation catheter combines Euphora technology with controlled, high-pressure performance.
Balloon Dilatation Catheter
OVERVIEW
From Collaboration to Innovation
When it comes to controlled, high-pressure performance, the NC Euphora™ noncompliant balloon dilatation catheter has what you’re looking for:
- High RBP up to 20 atm
- Low-growth profile1
- Superior deliverability1
In fact, we worked with nearly 2,000 interventional cardiologists and cath lab professionals to develop it — so you can choose it with confidence for your patients.
PRODUCT DETAILS
Looking for NC Euphora Noncompliant Performance?
ORDERING INFORMATION
BALLOON LENGTHS 6, 8, AND 12 MM
Balloon
Diameter
(mm)Balloon Length (mm) 6 8 12 2.00 NCEUP2006X NCEUP2008X NCEUP2012X 2.25 NCEUP22506X NCEUP22508X NCEUP22512X 2.50 NCEUP2506X NCEUP2508X NCEUP2512X 2.75 NCEUP27506X NCEUP27508X NCEUP27512X 3.00 NCEUP3006X NCEUP3008X NCEUP3012X 3.25 NCEUP32506X NCEUP32508X NCEUP32512X 3.50 NCEUP3506X NCEUP3508X NCEUP3512X 3.75 NCEUP37506X NCEUP37508X NCEUP37512X 4.00 NCEUP4006X NCEUP4008X NCEUP4012X 4.50 — NCEUP4508X NCEUP4512X 5.00 — NCEUP5008X NCEUP5012X BALLOON LENGTHS 15, 20, AND 27 MM
Balloon
Diameter
(mm)Balloon Length (mm) 15 20 27 2.00 NCEUP2015X NCEUP2020X — 2.25 NCEUP22515X NCEUP22520X — 2.50 NCEUP2515X NCEUP2520X NCEUP2527X 2.75 NCEUP27515X NCEUP27520X NCEUP27527X 3.00 NCEUP3015X NCEUP3020X NCEUP3027X 3.25 NCEUP32515X NCEUP32520X NCEUP32527X 3.50 NCEUP3515X NCEUP3520X NCEUP3527X 3.75 NCEUP37515X NCEUP37520X NCEUP37527X 4.00 NCEUP4015X NCEUP4020X NCEUP4027X 4.50 NCEUP4515X NCEUP4520X — 5.00 NCEUP5015X — — -
PTCA BALLOON ACCUFORCE
Description
Force. Success. No Compromise.
The great balance between high pressure and high resistance, accurate dilatation and advanced deliverability. Accuforce is the latest generation of non-compliant PTCA balloons.
Characteristics
- Provides impressive high-pressure resistance up to 22 atm
- Optimizes (re)crossability and deliverability1
- Operates accurately in pre- and post-dilatation
General specifications
Shaft diameter 1.9 Fr / 0.64 mm Proximal
2.5 Fr / 0.84 mm Mid
2.6 Fr / 0.86 mm DistalUsable length 145 cm Balloon markers 2 Nominal pressure 12 atm / 1216 kPa Rated burst pressure 22 atm / 2229 kPa (2.0 mm to 4.0 mm)
20 atm / 2026 kPa (4.5 and 5.0 mm)Guidewire compatibility Maximum diameter 0.014″ / 0.36 mm Lesion entry profile 0.43 mm Coating Hydrophilic Item specifications
Ordering Information
Balloon
diameter
(mm) Balloon length (mm) / Item references 6 8 12 15 20 25 30 2.00 DC-RM2006HSW DC-RM2008HSW DC-RM2012HHW DC-RM2015HHW DC-RM2020HHW — — 2.25 DC-RM2206HSW DC-RM2208HSW DC-RM2212HHW DC-RM2215HHW DC-RM2220HHW — — 2.50 DC-RM2506HSW DC-RM2508HSW DC-RM2512HHW DC-RM2515HHW DC-RM2520HHW DC-RM2525HHW DC-RM2530HHW 2.75 DC-RM2706HSW DC-RM2708HSW DC-RM2712HHW DC-RM2715HHW DC-RM2720HHW — — 3.00 DC-RM3006HSW DC-RM3008HSW DC-RM3012HHW DC-RM3015HHW DC-RM3020HHW DC-RM3025HHW DC-RM3030HHW 3.25 DC-RM3206HSW DC-RM3208HSW DC-RM3212HHW DC-RM3215HHW DC-RM3220HHW — — 3.50 DC-RM3506HSW DC-RM3508HSW DC-RM3512HHW DC-RM3515HHW DC-RM3520HHW DC-RM3525HHW DC-RM3530HHW 3.75 DC-RM3706HSW DC-RM3708HSW DC-RM3712HHW DC-RM3715HHW DC-RM3720HHW — — 4.00 DC-RM4006HSW DC-RM4008HSW DC-RM4012HHW DC-RM4015HHW DC-RM4020HHW — — 4.50 DC-RM4506HSW DC-RM4508HSW DC-RM4512HSW DC-RM4515HSW — — — 5.00 DC-RM5006HSW DC-RM5008HSW DC-RM5012HSW DC-RM5015HSW — — — Please quote above item reference codes when placing an order.
Balloon Compliance
Balloon
diameter
(mm) Pressure (atm) 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 2.00 1.58 1.65 1.72 1.79 1.84 1.88 1.92 1.95 1.98 2.00* 2.01 2.03 2.04 2.05 2.06 2.08 2.09 2.10 2.12 2.13** 2.14 2.15 2.17 2.25 1.96 2.01 2.06 2.11 2.14 2.16 2.19 2.21 2.23 2.25* 2.26 2.28 2.29 2.31 2.32 2.34 2.35 2.36 2.38 2.39** 2.41 2.42 2.44 2.50 2.19 2.24 2.30 2.36 2.38 2.41 2.44 2.46 2.48 2.50* 2.52 2.53 2.55 2.56 2.58 2.60 2.61 2.63 2.64 2.66** 2.68 2.69 2.71 2.75 2.43 2.48 2.53 2.59 2.62 2.65 2.67 2.70 2.73 2.75* 2.77 2.79 2.80 2.82 2.84 2.86 2.87 2.89 2.91 2.93** 2.94 2.96 2.98 3.00 2.65 2.71 2.76 2.82 2.85 2.89 2.92 2.95 2.97 3.00* 3.02 3.04 3.06 3.08 3.10 3.11 3.13 3.15 3.17 3.19** 3.21 3.23 3.25 3.25 2.89 2.95 3.01 3.07 3.10 3.14 3.17 3.20 3.22 3.25* 3.27 3.29 3.31 3.33 3.35 3.37 3.39 3.42 3.44 3.46** 3.47 3.48 3.51 3.50 3.13 3.19 3.26 3.32 3.35 3.39 3.42 3.45 3.47 3.50* 3.52 3.54 3.57 3.59 3.61 3.63 3.65 3.68 3.70 3.72** 3.74 3.74 3.76 3.75 3.37 3.44 3.50 3.56 3.60 3.63 3.66 3.69 3.72 3.75* 3.77 3.80 3.82 3.84 3.86 3.88 3.90 3.92 3.94 3.96** 3.98 3.99 4.01 4.00 3.58 3.65 3.72 3.79 3.83 3.87 3.90 3.94 3.97 4.00* 4.03 4.05 4.07 4.09 4.11 4.13 4.15 4.17 4.19 4.21** 4.23 4.26 4.28 4.50 4.02 4.10 4.19 4.28 4.32 4.37 4.40 4.44 4.47 4.50* 4.53 4.56 4.59 4.63 4.66 4.68 4.71 4.75** 4.78 4.81 4.84 4.87 4.91 5.00 4.52 4.59 4.67 4.75 4.80 4.85 4.89 4.93 4.96 5.00* 5.03 5.07 5.10 5.13 5.16 5.19 5.22 5.26** 5.29 5.32 5.35 5.38 5.41 * Nominal pressure
** Rated burst pressureReferences
1 Compared with Hiryu. Non-Compliant PTCA Balloon Catheter manufactured by Terumo Corporation.
Ordering Information. Balloon diameter (mm) , Balloon length (mm) / Item references .Balloon markers: 2Usable length: 145 cmCoating: HydrophilicLesion entry profile: 0.43 mmStraight-Single Latex Plastic Terumo Accuforce Balloon Catheter, Size: Medium ; Application, Hospital ; Brand, Terumo ; Material, Latex ; Inner Diameter, 36mm. -
Glide sheath
Product overview
Expanding trans-radial access to include more patients
- Glide sheath Slender is designed with a proprietary thin-wall technology where the outside diameter is reduced by one French size while the inner-diameter equivalent is maintained.
- Glide sheath Slender is coated with Terumo’s proprietary hydrophilic coating, allowing for smooth insertion and removal.
Features and Benefits

The proprietary thin-wall technology and Terumo M Coat hydrophilic coating
- Per the American Heart Association, dedicated radial sheaths with hydrophilic coating combined with smaller diameter sheaths and a tapered tip design may reduce risk of arterial spasm and radial occlusion1
- Featuring Terumo’s proprietary hydrophilic coating, the Glide sheath Slender Sheath is the only thin-wall radial sheath on the market to demonstrate superior and consistent performance in lubricity and durability over time
The Glide sheath Slender Sheath is the only thin-wall sheath that demonstrated best in class performance in all of the American Heart Association’s identified critical features that lead to reduced spasm.
THE POWER OF TERUMO GLIDE TECHNOLOGY™: LUBRICITY OVER TIMES
Hydrophilic coating is critical to procedural success, Physicians need to trust that their sheath will be just as lubricous at the end of case as it is at the beginning.
The graph below demonstrates the results of recent benchtop testing. The lower the value, the more lubricious the coating. The straighter the line, the more consistent, and reliable, the performance.
Glide sheath Slender Sheath outperformed the other competitive sheaths in both key features: lubricity and lubricity over time.

Unmatched Clinical Evidence
- A meta-analysis of 10 clinical papers, involving 3,821 patients, demonstrated that use of Glide sheath Slender Sheath is associated with high rates of procedural success and low rates in performance related issues.
- In studies measuring patient comfort, patients who underwent percutaneous trans-radial procedures with the Glide sheath Slender Sheath reported none to low amounts of pain.









35.01hvm0nt6jqdj62j0vs9tf1cmp@mail4u.fun –
nihil quisquam magni hic pariatur magni itaque voluptas voluptatum quia ad mollitia veniam et autem magni consequatur labore et rerum autem. quia quos sequi rem ea explicabo id quisquam. perspiciatis
Quiernera –
At higher concentrations, inhibition was observed buy priligy online