With multiple decades of experience in medical-grade polymers, we design, mould, and manufacture critical healthcare components that support patient care and medical innovation — from surgical instrument housings and diagnostic device parts to drug delivery components, sterile packaging, and implantable-grade elements.
Our focus goes beyond manufacturing — we engineer for regulatory compliance, cleanroom production, and validation requirements. Working with medical device OEMs, healthcare equipment manufacturers, and pharmaceutical companies, we produce components that meet strict tolerances, maintain sterility assurance levels, and integrate seamlessly with FDA-approved and CE-marked medical devices.
From IV components and syringe parts to diagnostic test housings, surgical tool handles, and medical equipment enclosures, our range is engineered for the exacting demands of healthcare applications. We understand the critical importance of material traceability, biocompatibility testing, and zero-defect manufacturing — and we build every part to deliver on all three.
OUR
EXPERTISE
We bring our expertise in medical-grade plastics, cleanroom molding, and regulatory compliance to the healthcare sector — helping clients achieve USP Class VI biocompatibility, ISO 10993 validation, and sterilization method compatibility. Our solutions support patient safety, regulatory approval pathways, and manufacturability under ISO 13485 quality management systems.
SURGICAL & PROCEDURAL COMPONENTS
We manufacture precision-molded medical components including surgical instrument handles, trocar housings, endoscopic device parts, laparoscopic tool components, biopsy device elements, and procedural kit assemblies designed for single-use and reusable medical applications. These parts are produced in ISO Class 7 & 8 cleanrooms using medical-grade polymers such as PEEK, Polysulfone, medical-grade PC, and biocompatible TPEs, ensuring dimensional accuracy, sterilization compatibility (autoclave, ETO, gamma radiation), and tissue-contact safety. Every product is engineered to meet FDA 510(k) requirements, ISO 13485 standards, and strict biocompatibility protocols for surgical and interventional procedures.
DIAGNOSTIC & LABORATORY SYSTEMS
From diagnostic test cassette housings and microfluidic components to specimen collection tubes, pipette tips, centrifuge parts, sample handling trays, and laboratory consumables, Jairaj offers solutions that ensure accuracy, contamination prevention, and consistent performance in clinical and research settings. Our components are designed to provide chemical resistance to reagents, optical clarity for detection systems, precise fluid handling geometries, and lot-to-lot consistency critical for diagnostic accuracy. These systems help medical device companies achieve regulatory clearance, maintain quality control, and ensure reliable test results across point-of-care and laboratory diagnostic platforms.
DRUG DELIVERY & PHARMACEUTICAL COMPONENTS
Jairaj produces inhaler components, syringe barrels and plungers, IV connectors, infusion pump parts, pen injector elements, vial adaptors, and custom pharmaceutical device assemblies for drug administration and therapeutic delivery systems. Our products are validated for drug compatibility, extractables and leachables testing, dose accuracy, bacterial barrier integrity, and compliance with USP requirements for pharmaceutical containers and closures. With capabilities to integrate sterile manufacturing, validation documentation, and design for manufacturability (DFM) support, we help pharmaceutical and medical device companies optimize drug delivery systems while meeting FDA, EMA, and global regulatory requirements for patient safety and therapeutic efficacy.
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LEADING THE WAY TO THE FUTURE
With advanced cleanroom manufacturing and medical polymer expertise, Jairaj delivers validated, regulatory-compliant components that meet global healthcare standards and advance medical device innovation. Let’s build safer, life-changing solutions — together.
