Engineered to exact customer specifications — no off-the-shelf dimensions, no compromises on biocompatibility, purity, or performance.
Our medical tubing is not a catalog item — it is a purpose-built solution, manufactured exclusively to your engineering drawings and functional requirements. Designed for critical healthcare applications including fluid transfer, wound drainage, irrigation, aspiration, and diagnostic sampling, every tube undergoes rigorous validation under ISO 13485 and ISO 9001 certified processes.
We do not stock standard sizes. There are no generic OD/ID/wall thickness values — because true medical-grade performance demands dimensional fidelity, material traceability, and process control unique to your device integration. “Medical tubing” isn’t just a term here — it’s the foundational specification.
No pre-defined dimensions — only your approved drawings drive production. From extrusion tooling to final packaging, every step is validated against your technical specifications.
Fully compliant with ISO 13485:2016 (medical device quality management) and ISO 9001:2015. Documentation, traceability, and change control are built into every batch.
Material selection (e.g., medical-grade PVC, silicone, TPE, PE), surface finish, kink resistance, and biocompatibility testing are prioritized per application — never compromised for cost or speed.
Used in surgical drains, chest tubes, and negative pressure wound therapy systems requiring precise flow dynamics and kink resistance.
Critical for urological, ophthalmic, and dental procedures where sterility, low particulate shedding, and consistent lumen integrity are non-negotiable.
Enables reliable blood, CSF, or tissue fluid transfer in analytical devices — optimized for minimal adsorption and dead volume reduction.
All resins sourced from FDA-listed suppliers; full CoA and extractables data provided per lot.
Laser micrometry and vision inspection applied to 100% of critical ID/OD/wall parameters — traceable to NIST standards.
USP Class VI testing, endotoxin limits ≤0.5 EU/mL, and particle count per ISO 14644-1 Class 7 cleanroom assembly.
We partner with OEMs, contract manufacturers, and R&D teams from concept through commercialization. Your drawing is our starting point — not a constraint.
Share your drawings, functional requirements, and target application — we’ll respond within 24 business hours with technical feasibility and quoting.