Specialised expertise where implantable systems demand more.

Controlled manufacturing for implantable systems.

Our manufacturing experience covers cleanroom assembly, implantable electronics, encapsulation, precision welding and the controlled processes required for long-term implantable devices.

Stimulation interfaces built on decades of experience.

Atrotech has practical experience in the design and manufacture of implantable stimulation electrodes and leads, including precise assembly and multipolar configurations.

A rare competence in transcutaneous energy transfer.

Inductive coupling is one of Atrotech’s most distinctive areas of expertise. We understand the complete link between external energy transmission and implanted receivers: coil geometry, alignment tolerance, coupling efficiency, system integration and practical use around implantable electronics.

This capability is particularly valuable for systems designed without an implanted battery, where reliability of the transcutaneous energy link is central to the architecture.

Robust encapsulation for long-term implantable reliability.

Atrotech has practical expertise in the industrialisation and encapsulation of implantable electronics, from component integration and package preparation to sealing, process control and verification.

For long-term implantable devices, the package is a critical barrier. Material selection, precision joining, hermetic sealing and validated manufacturing processes are integrated with the device architecture from the outset.

OEM manufacturing for implantable medical devices.

Atrotech provides OEM manufacturing and industrial subcontracting services for medical device companies, from development support and industrialisation to controlled series production.

Our capabilities combine implantable electronics, hermetic packaging, precision welding, cleanroom assembly, testing and traceability — with the confidentiality, quality discipline and regulatory awareness expected for high-value medical devices.

Engineering developed with the regulatory pathway in mind.

For an AIMD, regulatory strategy cannot be separated from design and manufacturing. Atrotech’s experience covers technical documentation, design verification and validation, risk management, clinical and post-market requirements, process validation and interaction with the European conformity-assessment pathway under MDR.