K-Yoddoogi (Mesh supporting the central urethra for the incontinence treatment)

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K-Yoddoogi (Mesh supporting the central urethra for the incontinence treatment) Price And Quantity

Minimum Order Quantity 1 Unit

Material Polypropylene mesh
Mesh Weight Lightweight design
Sterility Sterile
Type Central urethral support mesh
Product Name K-Yoddoogi (Mesh supporting the central urethra for the incontinence treatment)
Elasticity Optimized flexibility for patient comfort
Dimensions Customizable sizes available
Radiopacity Non-radiopaque
Usage Single-use
Storage Conditions Store in a cool, dry place away from sunlight
Pore Size Macroporous for tissue ingrowth
Application Surgical procedure for female urinary incontinence
Indication Stress urinary incontinence treatment
Packaging Individually packed in sterile container
Biocompatibility Tested to international standards
Shelf Life 5 years
Implantation Method Transobturator or retropubic approach

Product Description

K-Yoddoogi is a highly recommended opulent solution for addressing stress urinary incontinence through central urethral support. Crafted as a dazzling masterpiece of surgical innovation, this polypropylene mesh features customizable sizes, lightweight construction, and a macroporous design to highlight optimized tissue integration. Its elastic and flexible structure ensures optimal patient comfort, while access to both transobturator and retropubic implantation methods offers versatile surgical options. Rigorously tested for biocompatibility and delivered sterile in single-use packaging, K-Yoddoogi is highlighted for its safety, effectiveness, and long shelf life. Exported from Korea South.

Suitability and Application Surfaces

K-Yoddoogi's mesh is tailored for female patients requiring support for stress urinary incontinence. Its plant application is the surgical treatment of this condition, offering exceptional results on the central urethral surface. The mesh integrates seamlessly with the surrounding tissue, thanks to its macroporous and lightweight structure. Its optimized elasticity minimizes patient discomfort and promotes reliable healing, making K-Yoddoogi suitable for use in both transobturator and retropubic surgical procedures.

FOB Port, Sample, and Delivery Valuation

For international orders, K-Yoddoogi is dispatched from South Korea's leading FOB ports, ensuring efficient global access. Prospective clients may request product samples for a nominal charge, supporting thorough valuation and assessment before larger purchases. Standard delivery times are industry-competitive and depend on destination, with careful packaging ensuring the mesh arrives sterile and ready for immediate surgical application. Fast and secure shipping is highlighted as a key exporter commitment.

FAQ's of K-Yoddoogi (Mesh supporting the central urethra for the incontinence treatment):

Q: How is K-Yoddoogi mesh implanted during the treatment process?

A: K-Yoddoogi mesh can be implanted using either transobturator or retropubic approaches, allowing surgeons to choose the method best suited to the patient's anatomy and needs during stress urinary incontinence procedures.

Q: What are the benefits of the macroporous and lightweight design of K-Yoddoogi?

A: The macroporous, lightweight construction of K-Yoddoogi facilitates rapid tissue ingrowth, supports optimal patient comfort, and helps reduce foreign body sensation, contributing to effective and long-term incontinence management.

Q: When should K-Yoddoogi be considered for surgical intervention?

A: K-Yoddoogi should be considered for adult female patients diagnosed with stress urinary incontinence and who are seeking surgical options after conservative treatments have not provided sufficient relief.

Q: Where should K-Yoddoogi be stored before use?

A: Store K-Yoddoogi mesh in its sterile packaging, in a cool, dry environment away from direct sunlight, to maintain sterility and product integrity up to its five-year shelf life.

Q: What is the usage protocol for K-Yoddoogi?

A: K-Yoddoogi is a single-use product, individually packaged in sterile containers to ensure safety and sterility during each surgical procedure. It should be opened just prior to implantation.