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Find exciting articles about medical technology.

bbv Software Services AG

Hall 2 / E 2143

AI Consulting by bbv: How Healthcare and MedTech Benefit from Artificial Intelligence

Whether it’s precise diagnostics, efficient processes, or innovative digital services: Artificial intelligence is fundamentally transforming the MedTech and healthcare industry. bbv’s AI consulting helps companies seize these opportunities safely and practically – bringing together technology, data,

bbv Software Services AG

Hall 2 / E 2143

Swiss LCDM Hub: Seamless Interoperability for MedTech and Healthcare

Digital health data is pouring in from all directions – from hospital information systems, laboratory devices, or patient apps. The Swiss LCDM Hub by bbv brings order to this data chaos and enables seamless interoperability in the complex world of MedTech and healthcare.

bbv Software Services AG

Hall 2 / E 2143

Certainty for the future with the Rust Transition Service

Software development is evolving swiftly. Our Rust Transition Service secures, optimises and future-proofs your software. Especially in security-critical sectors like automotive, medical technology and finance, migrating to Rust helps meet regulations and significantly lower cyber attack risks.

CAQ AG Factory Systems

Hall 2 / C 2090

Quality management software that grows with you

CAQ.Net software solutions by CAQ AG facilitate a companywide quality mindset by offering solutions for the management of aspects such as processes, documents, trainings, audits, risks, complaints, and gauges as well as quality inspections.

EXCO Consulting GmbH

Hall 2 / D 2113

Regulatory-compliant validation of processes and methods

EXCO Consulting in Lucerne supports manufacturing MedTech and pharmaceutical companies in the regulatory-compliant validation of processes and methods - ensuring that reproducibility, reliability, and regulatory compliance are documented and verifiable.

EXCO Consulting GmbH

Hall 2 / D 2113

Regulatory-compliant qualification of systems and equipment

In the pharmaceutical industry, medical technology and in the clinical environment, the qualification of systems and equipment is a central component of GxP requirements.

Grossenbacher Systeme AG

Hall 2 / E 2146

Product life cycle: From development to end-of-life

Grossenbacher Systeme offers comprehensive life cycle management for electronic devices. With obsolescence management, spare parts storage, and redesign, we ensure the long-term availability of your products.

Grossenbacher Systeme AG

Hall 2 / E 2146

Production: Quality assurance and reliability

At Grossenbacher Systeme, we guarantee the highest quality and reliability in the production of medical electronics. From assemblies to complete devices – always in compliance with GMP, ISO 13485, and FDA standards. For safe, durable medical technology solutions.

Grossenbacher Systeme AG

Hall 2 / E 2146

Device development: innovation and compliance with standards

Innovative and standards-compliant device development for medical technology: At Grossenbacher Systeme, we combine state-of-the-art technologies with a systematic development process to create safe, regulatory-compliant medical devices.

NMI Naturwissenschaftliches und Medizinisches Institut an der Universität Tübingen

Hall 2 / B 2066

Wound monitoring using sensory nanofibers

To monitor the condition of chronic wounds, the dressing must be changed at short intervals. This delays wound healing and puts a strain on patients. In the WOUNDSENS project, NMI researchers want to develop innovative wound dressings that send information about the wound to the outside world.

thyssenkrupp Materials Schweiz AG

Hall 2 / B 2040

Sustainably reduce process costs with precision bars

We specialise in the most precise processes. A lot can be gained with precise surfaces and tolerances. With a little more input, you get up to three times more output. At the same time, reliable and reproducible processes will significantly increase profitability.

NMI Naturwissenschaftliches und Medizinisches Institut an der Universität Tübingen

Hall 2 / B 2066

MIK - MDR- & IVDR-Competence Centre

The strict regulations on medical devices (MDR) and in vitro diagnostics (IVDR) often pose major challenges for the industries concerned. As a competence center, MIK offers consulting and development capacities and is oriented towards the needs and requirements of the industry.

NMI Naturwissenschaftliches und Medizinisches Institut an der Universität Tübingen

Hall 2 / B 2066

NMI expertise for the highest medical standards

The NMI as a partner to innovative companies: An example of how this works can be seen in the surface finishing of medical devices, which is designed to make germs adhere less effectively to the instruments.

Elma Schmidbauer Suisse AG

Hall 2 / B 2056

Cleaning surgical Instruments – introducing an all-new Process

Clean surgical instruments in individual, cascaded small basins and then dry them by hand with a compressed air gun: This leads to the desired cleaning result, but is it economical and reproduceable?

Materialise NV

Hall 2 / D 2102

Why Sartorius Chooses Additive Manufacturing to Deliver Biocompatible Components

Discover how certified manufacturing at Materialise helps Sartorius deliver biocompatible and traceable parts to the highly regulated medtech industry.

TeSe AG

Hall 2 / A 2014

TwinTec cleaning and degreasing systems for medical devices

The hybrid solution for maximum cleanliness in medical technology. Our TwinTec technology offers unique flexibility in cleaning: both solvents and aqueous cleaning agents can be used in a single system.

TeSe AG

Hall 2 / A 2014

Aluminum adhesion with plasma & laser

Strong bonds, innovative solutions! Aluminum is lightweight but difficult to bond— until now. With our unique combination of plasma and laser treatment, we increase the adhesion of aluminum by up to 60%.

majesty GmbH

Hall 2 / C 2092

Your Digital Hub for Production Planning

With the Majesty Control Center, you always have full visibility of your production. Thanks to a graphical scheduling board, real-time data, and flexible planning tools, you can manage orders efficiently, avoid bottlenecks, and make optimal use of resources – ensuring smooth, on-time production.

majesty GmbH

Hall 2 / C 2092

The Digital Route Card: Always Keep an Eye on All Processes

With the digital route card in the Majesty Web Terminal, you can optimize your production and shipping processes – paperless, transparent, and in real time.

BIBUS AG

Hall 2 / C 2071

Our core competence in the life science sector

From standard products to customised solutions - our technical expertise enables cost-effective, high-performance fluid control and linear systems. We supply sophisticated, production-ready solutions that fulfil all technical and regulatory requirements.

Galvex GmbH

Hall 2 / F 2195

Two-Tone Titanium Innovation: Grey Meets Gold!

Experience at Medtec Luzern how delicate markings on titanium come to life like never before through our new two-tone anodizing in elegant grey and gold. Join us and be inspired!

Hohenstein Laboratories GmbH & Co.

Hall 2 / A 2032a

Efficacy and safety? Hohenstein Medical tests

The Hohenstein test spectrum includes softlines - textile materials -, hardlines - consumer goods made of solid materials - and medical products. As an accredited testing laboratory, Hohenstein Medical provides neutral proof of the effectiveness and safety of medical products.

Hepako - Präzisionsgummiartikel (Precision Rubber Parts)

Hall 2 / F 2197

Silicone & Rubber Micro Molding: Everything You Need to Know

Hepako GmbH from Raisting am Ammersee, Germany, specializes in the production of micro parts made of rubber or silicone. This opens up unique opportunities for their customers in medical technology.

majesty GmbH

Hall 2 / C 2092

Efficient Software Validation According to MDR

With majesty’s validation module, medical technology companies maintain full control over their ERP software at all times – MDR- and ISO 13485-compliant, time-saving, and audit-proof.