Anti-Counterfeiting Label Compliance Supply for Swiss Medical Device Company
Published On: March 25, 2026
The Swiss medical device industry is known for high quality and strict regulation. Product packaging must comply with MDR (Medical Device Regulation) requirements, ensuring traceability and anti-counterfeiting protection throughout the supply chain.
The client is a Zurich-based medical device distributor representing multiple international brands of high-value consumables. They faced risks of counterfeit products entering the market and needed enhanced packaging anti-counterfeiting and opening indication features.
Customized VOID tamper-evident labels using PET substrate and layered transfer technology, displaying "VOID OPENED" text upon removal that cannot be restored. Combined with holographic anti-counterfeiting patterns and microtext to increase forgery difficulty. Label materials passed biocompatibility testing, meeting medical device packaging requirements.
The client reported new labels effectively prevented unauthorized package opening, with end users able to visually identify product authenticity and opening status. Anti-counterfeiting labels enhanced brand protection and increased channel partner confidence.
Through multi-layer anti-counterfeiting technology, we helped medical device enterprises meet regulatory requirements while protecting brand value and patient safety.
