KIRAY Urology Portfolio

Urology Products for Global Healthcare Partners

The current KIRAY Medical portfolio focuses on urology medical devices for distributors, importers and healthcare organizations, supported by sourcing, documentation, private-label and export coordination.

KIRAY urology product portfolio
Procurement support

Product information matched to model and market

  • 4Current urology products
  • SizesConfigurations shown below
  • OEMPackaging and label options
  • DocsReviewed by model and market

Regulatory documentation is confirmed for the requested model and destination before use.

Urology Products

Explore KIRAY Medical’s current urology portfolio. Each verified product now has a dedicated page for specifications, packaging inquiries, documentation requests and related products.

Intermittent Catheters

Green connector and touch-free gripper detail of a hydrophilic intermittent catheter

Hydrophilic Intermittent Catheter

A sterile, single-use intermittent catheter with an integrated water sachet for activating the hydrophilic coating, available in multiple sizes, lengths and tip configurations.

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No-touch gripper detail of a ready-to-use intermittent catheter

Ready-to-use Intermittent Catheter

A sterile, pre-lubricated intermittent catheter supplied ready for use, with male, female and compact configurations available for B2B sourcing inquiries.

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Endourology

Complete hydrophilic ureteral access sheath and dilator set on a light background

Hydrophilic Ureteral Access Sheath

A hydrophilic-coated, reinforced ureteral access sheath designed to provide a stable working channel during ureteroscopic procedures.

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Complete hydrophilic coated J type ureteral stent set on a light background

Hydrophilic Coated J Type Ureteral Stent

A radiopaque medical-TPU J type ureteral stent available in hydrophilic-coated and uncoated configurations for model-specific sourcing inquiries.

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Regulatory & Quality Support

Documentation support for your product and market

Product- and market-specific regulatory documentation coordinated for distributors, importers and healthcare procurement partners.

FDA

US Regulatory Documentation

Supporting regulatory records are available for applicable products and configurations.

Model-specific applicability is confirmed upon request.

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CE

CE / EU MDR Documentation

Documentation status is reviewed by product, model and intended destination market.

Documentation availability to be confirmed.

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ISO 13485

Quality Management Documentation

Quality-management-system documentation relevant to the applicable manufacturing supply chain can be provided for verification where available.

Documentation availability to be confirmed.

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Regulatory documentation is product-, model- and market-specific. KIRAY Medical coordinates documentation verification as a supply and export partner and does not present itself as the legal manufacturer or certificate holder.

Current certificate validity, applicable product scope and EU Declaration of Conformity are confirmed before documentation is supplied for commercial or registration purposes.

Tell us what your market needs.

Share your preferred sizes, packaging, certification requirements and estimated volume. Our team will prepare a focused proposal.

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