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Endovascular cardiac products

Price 100 USD ($)/ Piece

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MOQ : 1 Piece

Endovascular cardiac products Specification

Measurement Range
Device diameter 1-6mm, Length 60-200cm

Function
Vascular Navigation, Stent Delivery, Cardiac Support

Display Type
N/A (used with compatible imaging systems)

Usage Type
Professional/Clinical

Instruments Type
Endovascular Instruments

Shelf Life
2-5 Years

Features
Flexible Design, High Precision Delivery, Biocompatible, Radiopaque Markers

Accuracy
High - Device placement under fluoroscopic guidance

Storage Instructions
Store in Clean, Dry, Sterile Conditions

Equipment Type
Endovascular Cardiac Product

Material
Medical-grade Polymer, Stainless Steel, Nitinol

Condition
New

Technology
Minimally Invasive Endovascular Technology

Portable
Yes

Wall Mounted
No

Magnification Power
Applicable via compatible imaging systems

Real-Time Operation
Supported

Noise Level
Low

Operating Type
Manual and Automated

Use
Cardiac and Peripheral Vascular Procedures

Power Source
Not required (Manual), Electric (for integrated devices)

Power Consumption
<10W (for powered instruments)

Voltage
110-240V (for powered units)

Dimension (L*W*H)
Varies by model; standard catheters: 150cm x 2.3mm

Weight
Approx. 12g to 100g depending on configuration

Color
Sterile White, Blue, Green Markings

Imaging Compatibility
Compatible with X-ray, CT, MRI guidance

Single Use
Yes

Working Channel
Available in 0.014" and 0.035" guidewire formats

Packaging
Sterile Blister Pack with Peel Pouch

Balloon Compliance
Non-Compliant, Semi-Compliant, Compliant (by model)

Pressure Rating
Rated up to 18 ATM (for balloon catheters)

Catheter Type
PTCA, PTA, Support Catheter, Delivery System

Temperature Tolerance
Up to 40°C operating

Radiopacity
Radiopaque markers for precision placement

Connection Type
Standard Luer Lock

Sterility
EO (Ethylene Oxide) Sterilized

Regulatory Approval
CE Mark, FDA 510(k) Cleared

Operator Training
Required for optimal results

About Endovascular cardiac products

Advin Endovascular Cardiac Products are a specialized line of sterile, single-use devices used for minimally invasive procedures within the heart and vascular system. This comprehensive range includes a variety of catheters, guidewires, and other accessories necessary for diagnostic and therapeutic interventions. These products are designed to ensure procedural safety, efficiency, and optimal patient outcomes.

Advanced Features:

Advanced Catheter Technology
Hydrophilic and PTFE Coatings
Radiopaque Markers
Kink-Resistant Materials
Ergonomic Design
Wide Product Range

Precision and Versatility in Cardiac Procedures

Engineered for both cardiac and peripheral vascular applications, our endovascular products combine flexible design with high radiopacity for precise placement. With available PTCA, PTA, support catheters, and delivery systems, clinicians benefit from exact navigation and stent deployment, supported by multiple balloon compliances to match procedure requirements.

Ensured Safety and Compliance

Each device is EO sterilized and supplied in a sterile blister pack with a peel pouch to prevent contamination. Backed by CE Mark and FDA 510(k) clearance, our products comply with international regulatory standards, ensuring both patient and practitioner safety during sensitive vascular interventions.

Seamless Compatibility and Operation

Simplify procedures with seamless compatibility across imaging systems-X-ray, CT, and MRI guidance assure real-time, high-accuracy placement. Standard luer lock fittings, radiopaque markers, and a choice of 0.014" or 0.035" guidewire formats facilitate broad procedural application and swift integration into existing workflows.

FAQ's of Endovascular cardiac products:

Q: How do I select the appropriate balloon compliance for my procedure?

A: Balloon compliance selection depends on the nature of the vascular lesion and procedural goals. Non-compliant balloons are best for precise dilation, semi-compliant for moderate flexibility, and compliant for delicate or tortuous vessels. Check device specifications and consult with your clinical guidelines.

Q: What is the process for ensuring sterility before usage?

A: All products are EO sterilized and packaged in sterile blister packs with a peel pouch. Before use, confirm the packaging integrity; open in a sterile environment right before the procedure to maintain sterility and prevent contamination.

Q: Where are these endovascular cardiac products commonly used?

A: These products are widely employed in hospital and clinical settings for cardiac and peripheral vascular procedures, including PTCA, PTA, and support for stent and device delivery under imaging guidance.

Q: What are the benefits of using devices with radiopaque markers?

A: Radiopaque markers provide clear visibility under X-ray, CT, or MRI, enabling the operator to achieve precise navigation and positioning, which reduces the risk of misplacement and enhances procedural outcomes.

Q: When is operator training required and what does it include?

A: Operator training is required before initial use to ensure optimal results. Training often covers device handling, compatibility with imaging systems, navigation techniques, safety protocols, and proper sterilization procedures.

Q: How should these products be stored to maximize shelf life?

A: Store the products in clean, dry, and sterile conditions at temperatures below 40C, away from direct sunlight and moisture. Following these instructions preserves their 2-5 year shelf life and maintains device integrity.

Q: What guidewire formats are available and which procedures are they suited for?

A: The products support both 0.014" and 0.035" guidewire formats. The 0.014" is ideal for coronary interventions and smaller vessels, while the 0.035" suits larger vessels and peripheral applications.

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