Medical
Biocompatible interconnect solutions for medical devices and healthcare applications — meeting stringent regulatory and performance requirements.
Critical Demands
Biocompatibility
Medical device components require biocompatible materials meeting ISO 10993 and USP Class VI standards for patient contact and implantable applications.
Sterilization
Devices must withstand repeated sterilization cycles — autoclave, gamma radiation, EtO gas and hydrogen peroxide sterilization methods.
Regulatory Compliance
Complete documentation and compliance to FDA, MDR and ISO 13485 requirements for medical device regulatory submissions and quality systems.
How We Deliver
Medical Wire
Biocompatible wire and cable with materials approved for medical device use. Low-outgassing materials for sensitive electronic equipment.
Miniature Connectors
Micro-D and nano connectors for space-constrained medical devices. Reliable contact systems maintain signal integrity in critical diagnostic equipment.
Clean Room Compatible
Materials suitable for clean room assembly and validated manufacturing processes meeting medical device quality requirements.
Regulatory Support
Technical documentation packages supporting FDA 510(k) submissions, MDR technical files and biocompatibility testing requirements.
From Design to Delivery
Supporting aerospace programmes from initial specification through to ongoing lifecycle support.
Device Development
Medical device engineers specify components during product development — biocompatibility requirements, sterilization compatibility and regulatory needs.
Material Selection
Our team provides biocompatibility data, sterilization compatibility and regulatory documentation supporting medical device development.
Validated Supply
Components supplied with material certifications, biocompatibility test reports and documentation for regulatory submissions.
Quality Support
Support for design verification, validation testing and ongoing quality requirements through product lifecycle and regulatory approvals.
