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Advanced PTCA Balloon Device

Price 55 USD ($)/ Piece

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MOQ : 1 Piece

Advanced PTCA Balloon Device Specification

Function
Expands narrowed arteries in PTCA procedures

Measurement Range
Balloon diameter: 1.5mm to 4.0mm

Storage Instructions
Store in cool, dry place below 25C

Features
High pressure, Rapid conformability, Minimal tip profile, Enhanced pushability, Kink resistance

Usage Type
Single Use / Disposable

Accuracy
Precision controlled inflation

Instruments Type
Interventional Cardiology

Shelf Life
3 Years

Equipment Type
PTCA Balloon Device

Material
Medical Grade Polymer

Condition
New

Technology
Advanced Balloon Angioplasty

Portable
Yes

Wall Mounted
No

Real-Time Operation
Yes

Noise Level
Silent Operation

Operating Type
Manual / Catheter-based

Use
Coronary angioplasty for dilatation of stenotic arteries

Power Source
Manual

Dimension (L*W*H)
Variable (Custom as per model)

Weight
Lightweight, <20 grams per unit

Color
Clear/Transparent with color code marker

Latex Content
Latex-free

Sterilization Method
Ethylene Oxide (EO) sterilized

Maximum Inflation Pressure
Up to 20 atm (varies by model)

Guidewire Compatibility
Compatible with 0.014" guidewire

Balloon Length Range
8 mm to 38 mm

Balloon Material
Semi-compliant or non-compliant polyamide or polyurethane

Coating
Hydrophilic on distal shaft, hydrophobic proximal body

Balloon Compliance
Semi-compliant / Non-compliant options available

Packaging
Sterile, double pouch system

Catheter Length
143 cm / 140 cm (standard)

Marker Bands
Dual radiopaque markers

Regulatory Certification
CE Marked / ISO 13485 certified

Crossability
Enhanced for complex lesion navigation

Tip Profile
Ultra-low tip (<0.017") for easy crossability

About Advanced PTCA Balloon Device

The advanced PTCA balloon device is designed to support precise and controlled dilation of coronary arteries during interventional cardiology procedures. Its construction allows predictable balloon expansion to help clinicians manage vessel narrowing effectively. Advin Health Care manufactures this device with a focus on clinical reliability, safety, and consistent performance. The device is suitable for routine and complex PTCA procedures, supporting efficient workflow and dependable procedural outcomes.

Advanced Features

Designed for controlled and uniform balloon expansion
Supports effective coronary artery dilation
Smooth balloon profile for safe vessel navigation
Compatible with standard PTCA guide wires and systems

Product Keywords
Advanced PTCA Balloon Device, PTCA Balloon Catheter, Coronary Angioplasty Balloon, Non-Compliant Balloon Catheter, High Pressure Balloon Catheter, Interventional Balloon Device

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Precision Engineering for Complex Interventions

Engineered with an ultra-low tip profile and dual radiopaque marker bands, this PTCA balloon device offers superior crossability and accurate placement, addressing complex and tortuous coronary lesions. The hydrophilic and hydrophobic coatings facilitate ease of advancement and withdrawal, minimizing procedural challenges in interventional cardiology.

Versatile Sizing and Controlled Inflation

With balloon lengths ranging from 8 mm to 38 mm and diameters between 1.5 mm and 4.0 mm, this device provides flexibility for a variety of lesion types. Its semi-compliant and non-compliant options, with inflation pressures up to 20 atm, enable meticulous angioplasty with minimal risk of vessel trauma.

Safe, Sterile, and Reliable Performance

Manufactured to the highest safety standards, the device is latex-free, EO sterilized, and presented in a sterile, double pouch. Lightweight and portable for single-use, it ensures patient safety, reduces cross-contamination risk, and supports demanding procedural schedules.

FAQ's of Advanced PTCA Balloon Device:

Q: How is the Advanced PTCA Balloon Device used during coronary angioplasty procedures?

A: The device is inserted over a 0.014" guidewire and advanced to the site of the stenotic coronary artery. Controlled inflation of the balloon, with pressure up to 20 atm depending on the model, dilates the artery to restore blood flow. The ultra-low tip and hydrophilic coating enhance navigation through complex lesions.

Q: What materials and design features contribute to the device's enhanced crossability and pushability?

A: Manufactured from semi-compliant or non-compliant polyamide or polyurethane and featuring an ultra-low tip profile of less than 0.017", the device offers excellent lesion crossability. The hydrophilic-coated distal shaft reduces friction, while the device's kink-resistant design and dual radiopaque markers promote optimal tracking and precise positioning.

Q: When should a semi-compliant versus a non-compliant balloon be selected?

A: Semi-compliant balloons are generally chosen for pre-dilation or when some degree of conformability is required, while non-compliant balloons are preferred for high-pressure post-dilation or cases needing precise vessel sizing and minimal balloon expansion beyond nominal diameter.

Q: Where can the Advanced PTCA Balloon Device be employed, and what regulatory standards does it meet?

A: This device is intended for interventional cardiology settings, specifically for percutaneous transluminal coronary angioplasty (PTCA) in hospitals or catheterization laboratories. It holds CE Marking and ISO 13485 certification, ensuring international quality and safety compliance.

Q: What benefits does the dual-marker band system offer during procedures?

A: The dual radiopaque markers improve visibility under fluoroscopy, allowing clinicians to precisely gauge balloon positioning relative to the lesion, which increases procedural accuracy and safety.

Q: How should the device be stored to maintain its integrity and shelf life?

A: Store the device in a cool, dry location, away from direct sunlight, at temperatures below 25C. Ensure it remains in its sterile, double-pouch packaging until point of use to maintain sterility and effectiveness throughout its 3-year shelf life.

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