Esophageal Uncovered SEMS for Stricture Relief - 18x120 mm

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Esophageal Uncovered SEMS for Stricture Relief - 18x120 mm

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Esophageal Uncovered SEMS for Stricture Relief - 18x120 mm Specification

Instruments Type
Minimally invasive medical device

Measurement Range
18 mm diameter, 120 mm usable length

Accuracy
High, conforms closely to esophageal walls

Shelf Life
Up to 3 years (unopened, as per manufacturers instruction)

Storage Instructions
Store in a cool, dry place away from direct sunlight

Function
Esophageal stricture relief, maintains patency

Usage Type
Single Use Only

Features
Excellent radial force, precise placement, fully uncovered, anti-migration design

Equipment Type
Esophageal Uncovered Self-Expandable Metal Stent (SEMS)

Material
Nitinol (Nickel Titanium Alloy)

Condition
New

Technology
Self-expandable Memory Alloy Technology

Portable
Yes

Wall Mounted
No

Real-Time Operation
Yes

Noise Level
Silent operation

Operating Type
Manual Deployment

Use
Stricture Relief for Esophageal Obstruction

Dimension (L*W*H)
18 mm diameter x 120 mm length

Weight
Lightweight (Precise value depends on stent dimensions)

Color
Metallic Silver

Latex Content
Latex-free

Packaging
Individually packed in sterile peel-open packs

Deployment System
Introduction system included for controlled release

Removal
Removable by endoscopic procedure when indicated

Flexibility
High conformability for tortuous anatomy

Patient Safety
Atraumatic rounded stent ends minimize tissue injury

Radiopacity
Radiopaque markers for accurate positioning under fluoroscopy

Indication
Benign and malignant esophageal strictures

Compatibility
Fits standard endoscope delivery systems

Corrosion Resistance
Excellent, suitable for long implantation periods

Sterilization Method
Sterile, provided in sealed packaging

About Esophageal Uncovered SEMS for Stricture Relief - 18x120 mm

The Esophageal Uncovered SEMS for Stricture Relief 18120 mm is used in endoscopic treatment of esophageal strictures and obstructions that restrict swallowing. Its self-expanding metal mesh design provides reliable and uniform lumen opening while maintaining flexibility for patient comfort. The uncovered configuration promotes tissue integration, offering strong anchorage and reducing the chances of stent migration during therapy. Radiopaque markers improve visibility under imaging, ensuring precise endoscopic placement. Advin Health Care supplies this stent with dependable quality suitable for advanced gastrointestinal and esophageal interventions.

Advanced Features:

Uncovered design for secure tissue integration
Self-expanding metal mesh for smooth deployment
Flexible construction for improved patient comfort
Radiopaque markers for accurate placement

Advanced Radiopaque Guided Placement

Radiopaque markers are integrated into the stent, enabling accurate visualization and positioning under fluoroscopy during the procedure. This ensures precise alignment at the site of esophageal obstruction, reducing the risk of misplacement and facilitating a smooth clinical workflow for physicians performing minimally invasive interventions.

Engineered for Flexibility and Patient Safety

With high conformability, this stent adapts effortlessly to irregular esophageal contours and tortuous anatomical pathways. The atraumatic rounded ends further ensure minimal risk of tissue injury or discomfort, providing safe, effective, and gentle stricture relief for both benign and malignant esophageal conditions.

Fully Compatible and Convenient for Clinical Use

Supplied sterile in individually peel-open packs, this lightweight stent is designed for use with standard endoscope delivery systems. Its anti-migration and corrosion-resistant properties allow for prolonged implantation, while endoscopic removability supports tailored patient care. The single-use device streamlines handling and reduces infection risks.

FAQ's of Esophageal Uncovered SEMS for Stricture Relief - 18x120 mm:

Q: How is the Esophageal Uncovered SEMS positioned during the procedure?

A: The stent is equipped with radiopaque markers to help physicians achieve accurate placement under fluoroscopy. It is deployed through an integrated introduction system, ensuring precise and controlled release at the targeted site.

Q: What are the primary uses for this stent?

A: This SEMS is indicated for relieving strictures of the esophagus, whether benign or malignant. It is effective in restoring patency and improving swallowing for patients with obstructive esophageal conditions.

Q: When should the stent be removed, and how is this done?

A: The stent may be removed by a physician using an endoscopic procedure when clinically indicated, such as upon resolution of the stricture or when repositioning is necessary. Removal is minimally invasive and typically well tolerated.

Q: Where should the stent be stored prior to use?

A: The unopened stent should be stored in a cool, dry place away from direct sunlight to maintain its sterility and integrity. The packaging is sterile and designed for single-use only.

Q: What benefits does the nitinol construction provide?

A: Nitinol offers excellent corrosion resistance and self-expandable memory alloy properties, allowing the stent to conform closely to the esophageal walls and maintain radial force, supporting long implantation periods and reliable patency.

Q: How does the stent ensure patient safety during and after placement?

A: Its atraumatic, rounded ends are designed to minimize tissue injury, while its anti-migration design helps prevent displacement. The stent is also latex-free, reducing the risk of allergic reactions.

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