Princess® Lift portfolio rejuvenationNew name “Princess® Threads”- New CE Mark - 3 new suture subtypes
Croma strives for bringing innovations to maximize its customers and patient's well-being. As an expert in the combination of different technologies Croma offers a steadily growing, well-coordinated aesthetic product portfolio. Many years of experience in medical devices in aesthetic medicine enables Croma to successfully master the current regulatory challenges caused by the new European Medical Device Regulation. For this reason, we have further developed the portfolio of the Croma bestseller Princess® Lift.
Most suture manufacturers affected by the new MDR
Europe's new Medical Device Regulation (MDR) will cause substantial changes to the way medical device manufacturers register their products to the European market, and how they maintain compliance throughout the product's life cycle (technical documentation, product safety, clinical evaluation, post-market clinical follow-up, traceability). Since the sutures that are currently marketed in Europe are registered as medical device, they will all be affected by the new regulation. For many suture manufacturers, the regulatory requirements will be difficult to implement.
Croma is a step ahead of competition
In the partnership with our manufacturer we have managed to transfer the production of our well known Princess® Lift sutures to the new production site, which 100% complies with the new MDR. In addition, the product name has been changed to Princess® Threads. The new production site also opens for us a technical possibility to introduce 3 new subtypes on top to the existing ones.