Medical Tubing Solutions

Aokeray manufactures precision medical tubing for catheter and minimally invasive device applications.

Our capabilities include:

From prototyping to volume production, we support your project at every stage.

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Engineering Support for Your Tubing Project

Work directly with our extrusion engineering team on material selection, tolerance review and custom tubing development.
Whether you’re building a new catheter or optimizing an existing design, we help you move faster from concept to production.Typical response time: within 24–48 hours.
Built to support both prototyping and large-scale production.

40+ extrusion production lines
24/7 manufacturing operation
Fast sampling supportStable lead times
Tight dimensional control
100% inspection for critical dimensions

Material Knowledge & Application Insights

We continuously study fluoropolymer materials for medical extrusion applications.

Explore technical articles on:

  • PTFE liner performance
  • FEP heat shrink processing
  • Pebax material selection
  • Catheter shaft construction
  • Surface treatment & grabando
  • ISO 13485,USP Class VI,ROHS,ALCANZAR
    Original verification

Built from real manufacturing experience and project feedback

PTFE Tube & PTFE heat shrink

Thin-wall PTFE liner tubing for catheter shaft construction.

Designed for low friction performance, guidewire compatibility and smooth inner lumen.

Available in custom ID, OD and wall thickness for interventional catheter applications.

Etching PTFE

Etched PTFE liner tubing for improved bonding in catheter shaft assembly.

Surface treatment improves adhesion between PTFE and outer jacket materials.

Used in braided catheter shafts and multilayer tubing structures

FEP Heat Shrink Tube

Medical grade FEP heat shrink tubing for catheter lamination and reflow processing.

Provides uniform shrink performance, transparency and clean release after heating.

Suitable for balloon bonding, shaft lamination and braid reinforcement applications.

Multi-Lumen Tubing

Custom multi-lumen medical tubing for fluid delivery, guidewire access and device integration.

Extruded with precise lumen geometry and dimensional control.

Available in custom profiles for catheter and minimally invasive device application

PEBAX Liner

Pebax extrusion tubing for flexible catheter shafts and multi-layer device construction.

Combines flexibility, pushability and kink resistance.

Available in multiple hardness grades and custom extrusion configurations.

Peelable Heat Shrink Tubing

Peelable heat shrink tubing designed for catheter manufacturing and reflow processing.

Easy to remove after heating without damaging the shaft surface.

Suitable for applications requiring clean peel and consistent forming results

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ABOUT AOKERAY POLYMER TECHNOLOGY

Aokeray is a medical tubing manufacturer specialized in fluoropolymer extrusion for catheter applications.

With years of experience in PTFE, FEP and Pebax processing, we supply tubing solutions to medical device companies worldwide—from early-stage development through full-scale production.

Our focus is simple:

  • reliable quality
  • precise dimensions
  • responsive engineering support
  • dependable delivery

We help customers build better catheter devices with consistent tubing performance.

Why Medical Device R&D Engineers Partner with Aokeray:

  • Engineering & Development Capability

    Our engineering team focuses on advanced polymer extrusion for medical applications.

    Core expertise includes:

    • Ultra-thin wall PTFE liners
    • Tubo termorretráctil FEP
    • Multi-layer catheter tubing
    • Surface etching technology
    • Custom profile extrusion

    We work closely with customers to improve manufacturability, performance and production efficiency.


Clinical Specialties & Device Applications

Aokeray’s high-concentricity fluoropolymer extrusions and precision-etched liners are qualified across a broad spectrum of minimally invasive therapeutic areas. Our components are custom-engineered to meet precise torsional stiffness, trackability, and biocompatibility requirements demanded by modern interventional medicine.

Cardiovascular and Peripheral Device Components

PTFE liners, heat-shrink tubing and related components may be evaluated for catheter shaft, delivery-system and sheath manufacturing. Feasibility depends on the drawing, material grade, muro, tolerancia, surface condition and assembly process.

Final lumen, profile, deployment and device performance must be verified in the customer’s complete design.

optimizing catheter trackability

Neurovascular Device Components

Historical or project-specific test data may include inner-surface static/dynamic friction values at or below 0.08 under the stated sample preparation and test method. The result is not a universal product guarantee and must be reconfirmed for the selected resin, dimensiones, surface and test conditions.

Torque response, kink resistance and guidewire or coil delivery performance depend on the complete shaft construction and finished-device validation.

complex surgical shafts

Endoscopy and Fluid-Path Components

PTFE, FEP and multi-lumen tubing may be evaluated for instrument channels, fluid paths and protected components. Specify the medium, dimensiones, repeated-use conditions, cleaning or sterilization method and acceptance tests.

Material and process compatibility must be confirmed for the actual device and use conditions.

fep fluid delivery line01

Electrical and Thermal Isolation Components

Selected PTFE/FEP heat-shrink configurations may be discussed with shrink ratios up to 4:1, subject to product size, material and recovery conditions. Raw-material or project data may reference dielectric strength of 500 V/mil or greater when tested under the stated ASTM D149 conditions.

These figures are not blanket finished-component or device ratings. Confirm the exact product, muro, conditioning, electrodes, test environment and assembly validation.

ptfe fep delivery lines

Design and Verification Support

Aokeray can review material, geometría, manufacturability, inspection and documentation requirements for a tubing component. The quotation identifies the proposed product and project-specific evidence that can be supplied.

Regulatory submissions, clinical claims and finished-device validation remain the device manufacturer’s responsibility unless a separate written agreement defines another scope.

Discuss your application with an extrusion engineer

16 Millón $

Reported Revenue Reference*

80

Clients Worldwide Reference*

10

R&D Engineers Reference*

20 Años

Years of Experience Reference*

Engineering-Led Medical Polymer Tubing

Custom PTFE, FEP and Pebax tubing for catheter, medical-device and industrial projects.

Specify dimensions, material grade, tolerancias, surface condition and inspection requirements for a drawing-based feasibility review.

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Controlled Environment Manufacturing & Full Traceability

Aokeray operates fluoropolymer and thermoplastic extrusion lines in controlled-environment areas. The current quality-management certificate, its issuing body, site and scope should be reviewed during supplier qualification; ISO 13485:2016 wording applies only to the scope shown on the current certificate.

Raw Material Integrity

  • Virgin-resin requirements are available for selected projects where specified on the drawing or purchase order.
  • USP Class VI and FDA 21 CFR 177.1550 references, where available, apply to the named resin grade and stated conditions of use. They are not blanket approval of every finished tube or device.
  • Resin lots can be recorded and linked to the supplied component according to the agreed traceability plan.

Batch Traceability

For projects requiring lot traceability, Aokeray can document links between the applicable resin lot, production lot and packaging label. The original two-hour complaint-trace target is a project capability target and should be confirmed in the quality agreement, including records access, product scope and response conditions.

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precision metrology
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Empirical Quality Control Protocols & Batch Testing

For selected projects, batch-release testing may include physical, dimensional, surface or thermal checks defined in the drawing and inspection plan. The listed values and methods are retained as available project data and are not automatic release criteria for every tube.

Verification parameter Available method or reference Project-specific acceptance
Surface energy (grabando) Automated goniometer contact-angle analysis Contact angle < 70° and >5 N/cm bonding-strength references may be used only when the liner, tratamiento, bond stack and test method are stated in the approved project specification.
Mechanical properties Digital tensile testers; ASTM D638 / D3801 references Tensile strength and elongation are confirmed for the named material, geometría, conditioning and agreed sample plan.
Thermal performance Calibrated forced-air convection ovens Longitudinal shrinkage ≤ ±5% may be an agreed heat-shrink project criterion; confirm the tube, ciclo de calor, conditioning and measurement method.
Visual integrity 20×–40× stereo zoom microscopic inspection Micro-fracture, delamination and processing-mark criteria are defined by the drawing or appearance standard; zero-defect language requires an agreed inspection scope and sampling plan.

Specific test reports, equipment records and acceptance criteria are confirmed in the quotation, inspection plan or quality agreement.

Solicitar una revisión de dibujo

Send your tubing drawing, material, dimensiones, prototype quantity and quality-document requirements.

Sample and Stock Options

Ask about available standard sizes, evaluation samples and repeat-order supply options.

Engineering Collaboration

Work with Aokeray engineers to review material, geometría, processing and inspection requirements for your tubing project.

Tubo médico flexible Aokeray

Discuss Your Medical Tubing Project

Supplier Support for Medical-Device Development

Aokeray works with catheter, minimally invasive-device and medical-component teams on drawing-based tubing projects. Customer names and project details are treated as confidential unless written publication permission is provided.

Remote supplier reviews and scheduled manufacturing-site visits can be discussed during qualification.

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