Unlike conventional methods, which apply NFC tags via adhesive or assembly to external elements such as labels, Linxens and Clayens have chosen to innovate by integrating the NFC tag directly into the polymer matrix of the medical device. This approach allows for the tag to be inseparably fused with the product, offering unprecedented security through an unfalsifiable Unique Identifier (UiD).
At the heart of this initiative is the development of a revolutionary mini-tag, directly moulded into the polymer of the medical device. This circular tag combines durability and discretion through the use of a flexible polymer substrate enriched with copper loops and an integrated chip.
The encapsulation process, which involves a double overmoulding (first the overmoulding of the tag, and then the overmoulding of the new insert), ensures resistance to moisture, heat, and chemicals, offering unmatched reliability for demanding medical environments.
Critical information, such as expiration date, lot number, and dosage information, is programmed onto the NFC tag immediately after moulding. This crucial step takes place during the industrialisation process, using a specialised NFC writing device that ensures constant traceability and increased security against counterfeiting and unauthorised removal.
The mini-tag strictly complies with regulatory standards for medical devices and syringes, including the European Directive on Counterfeit Medicines, ensuring complete compatibility with existing inventory or tracking systems.
"Linxens, a historical leader in micro-connectivity technologies, is positioning itself strongly in the health sector, bringing technology and expertise that find their full meaning in this context," said Yvan Malépart, SVP Healthcare & Smartcard at Linxens. "Global health challenges demand the convergence of technical and clinical expertise, with a growing need for remote monitoring, secure connections, data quality, in an aging population, increasing patient autonomy, and overburdened healthcare services. By partnering with Clayens, Linxens is committed to addressing the demands of a constantly evolving market and a dynamic innovation landscape. With this revolutionary mini-tag, Linxens offers a solution that embraces cutting-edge technological advancements, ensuring reliability, enhanced security, and unmatched traceability in the administration of treatments."
"Working with Linxens on the integration of this mini-tag marks a significant step towards safer and more traceable medical devices," said Matthieu Besse, R&D Manager at Clayens. "This collaboration is a tangible example of our ability to integrate advanced technological innovations directly into our products, while maintaining our commitment to quality and security."
Linxens and Clayens collaborate to develop a Mini NFC Tag
In a significant advance for the medical sector, Linxens, a pioneer in the design and manufacturing of electronic components, is collaborating with Clayens, a European leader in the transformation of polymers, composites, and precision metal parts, to develop a unique medical tracker directly integrated into the material
You may also like
Manufacturing
BD and Suttons Creek collaborate to streamline combination product development for pharma and biotech
Read moreThe new strategic collaboration will help pharmaceutical and biotech companies reduce development risk and regulatory complexity across drug-device combination products, including biologics and GLP-1 therapies
Trending Articles
You may also like
Manufacturing
BD and Suttons Creek collaborate to streamline combination product development for pharma and biotech
The new strategic collaboration will help pharmaceutical and biotech companies reduce development risk and regulatory complexity across drug-device combination products, including biologics and GLP-1 therapies
Regulatory
FDA grants Orphan Drug Designation to pegrizeprument for prevention of heart transplant rejection
The FDA has granted Orphan Drug Designation to pegrizeprument (VEL-101), a novel monoclonal antibody fragment licensed to Veloxis Pharmaceuticals, for the prevention of heart allograft rejection, following a similar designation granted for liver transplant rejection in January 2026
Manufacturing
Cipla receives FDA approval for first AB-rated generic of Ventolin HFA in $1.5bn US albuterol market
Indian pharmaceutical company Cipla has secured final FDA approval for its Albuterol Sulfate Inhalation Aerosol, becoming the first AB-rated generic therapeutic equivalent of GlaxoSmithKline's Ventolin HFA
Manufacturing
Freudenberg Medical launches CleanAssure ISO Class 5 cleanroom service for sterile single-use biopharma assemblies
CleanAssure is an ISO Class 5 controlled cleanroom service delivering washed, dried and gamma-sterilised single-use assemblies to biopharmaceutical customers, addressing industry challenges around cleaning validation and contamination risk
Manufacturing
Mabwell signs Malaysia licensing deal for denosumab biosimilars MAILISHU and MAIWEIJIAN
Mabwell has entered a licensing and commercialisation agreement to bring its denosumab biosimilars to Malaysia, supporting regional access through local registration and supply of its Prolia and Xgeva reference products