Hot Sale Surgical Lumen Central Venous Catheter Set Price
Material: Radiopaque Polyurethane
Certification: CE Marked / ISO 13485
Certification: CE Marked / ISO 13485
Manufactured in Class 100,000 cleanrooms with certified biocompatibility, full batch traceability, and custom dimensional tolerances for demanding clinical environments in Austria.
The Austrian healthcare sector—anchored by world-renowned university clinics such as AKH Wien (Vienna General Hospital) and premier MedTech technology clusters in Upper Austria (MedTech-Cluster) and Styria (Human Technology Cluster)—maintains some of the strictest standards for single-use medical devices and surgical fluid-handling systems in Europe.
As a seasoned manufacturer and exporter of medical-grade tubing, silicone profiles, and surgical cannulated systems, Sterimed Group supplies high-purity medical tubing designed to fulfill the complex bio-mechanical requirements of modern clinical procedures. From micro-extruded multi-lumen central venous catheters to platinum-cured silicone peristaltic pump tubing, our production processes combine cleanroom manufacturing under ISO 13485 with rigorous batch validation.
"Precision medical extrusion for Austrian importers demands strict compliance with EU Regulation 2017/745 (MDR), phthalate-free biopolymer formulation, and verifiable Ethylene Oxide (EO) sterilization residuals per ISO 11135."
Whether catering to hospital procurement groups, surgical instrument OEMs, or pharmaceutical bioprocessing lines across Vienna, Linz, Graz, and Innsbruck, our engineering desk offers customizable durometer specifications, radiopaque longitudinal striping, kink-resistant braid reinforcements, and custom tip geometries tailored for seamless integration.
Comprehensive material classification engineered to assist Austrian biomedical engineers and procurement teams in identifying optimal tubing properties for specific clinical applications.
| Polymer / Material | Shore Hardness Range | Biocompatibility Standard | Sterilization Compatibility | Primary Clinical Application in Austria |
|---|---|---|---|---|
| Platinum-Cured Silicone (Ultrasil) | Shore A 30 to Shore A 80 | ISO 10993 / USP Class VI | Autoclave, Gamma, EO, Steam | Pharma bioprocessing, peristaltic pumps, surgical drainage, long-term implants. |
| DEHP / Phthalate-Free Medical PVC | Shore A 55 to Shore A 98 | ISO 10993-5 / REACH Compliant | Ethylene Oxide (EO), Gamma | IV infusion sets, respiratory therapy, Foley catheter shafts, suction lines. |
| Thermoplastic Polyurethane (TPU) | Shore A 70 to Shore D 75 | ISO 10993-10 / 11 | EO Gas, Electron Beam | Central venous catheters, arterial lines, micro-luminal surgical access tubes. |
| Reinforced Stainless Steel 316L / Cannula | High Structural Rigidity | ASTM F138 Medical Grade | Autoclave, Dry Heat, EO | Laparoscopic trocars, veterinary surgical cannulae, ENT endoscopic probes. |
Our tailored extrusion lines serve specialized health infrastructure sectors across Austrian states, maintaining operational excellence from acute care to medical device assembly.
Supplying acute care centers like AKH Wien and Landeskrankenhaus Graz with high-flow lumen catheters, siliconised endotracheal tubes, and closed-system suction lines that satisfy rigorous Austrian hospital hygiene protocols.
Partnering with medical equipment manufacturers in Linz, Wels, and Salzburg requiring specialized tubing configurations—including co-extruded multi-layered tubing, radiopaque lines, and micro-bore dimensions down to 0.2mm ID.
Providing Ultrasil platinum-cured silicone tubing for high-purity bioprocessing facilities across Vienna’s Biotech Cluster, featuring non-pyrogenic properties, low extractables, and full cleanroom documentation.
With the full implementation of the European Union Medical Device Regulation (EU MDR 2017/745), medical device importers and distributors in Austria face heightened scrutiny regarding material composition, biocompatibility dossiers, and supply chain integrity.
Regulatory authorities such as AGES (Austrian Federal Office for Safety in Health Care) and BASG (Federal Office for Safety in Health Care) enforce strict vigilance on plasticizers and endocrine-disrupting chemicals. The Austrian medical industry is actively transitioning away from traditional DEHP-plasticized PVC toward eco-friendly, phthalate-free PVC formulations, Thermoplastic Elastomers (TPE), and medical-grade Silicone.
Sterimed Group provides fully compliant Technical Documentation Files (TDF) for all supplied medical tubing and surgical sets. Our products are supported by complete ISO 10993 biocompatibility testing, physical testing verification (burst pressure, tensile strength, flow rate consistency), and validated shelf-life stability studies.
Combining over six decades of manufacturing history with modernized cleanroom automation to deliver unmatched cost efficiency and regulatory assurance for Austrian clients.
Operates under audited Quality Management Systems ensuring consistent medical device conformity per international standards.
Custom precision mold-making and micro-extrusion lines capable of maintaining ultra-tight dimensional tolerances.
Extensive international logistics experience shipping to major European hub ports (Hamburg, Koper) and Vienna International Airport.
End-to-end custom branding, multilingual IFU creation, and customized retail or sterile blister pouch packaging configurations.
Addressing common technical, regulatory, and logistics queries encountered by procurement departments in Austria.
Connect directly with our international regulatory desk and senior extrusion engineers to discuss your product requirements, request free sample kits, or obtain technical dossier files.
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