TMRW Vault® Gains CE Mark Under EU Medical Device Regulation

Reprotech, LLC announced that its TMRW Vault® has secured the CE marking as a Class IIa medical device under Regulation (EU) 2017/745. This certification facilitates the device's commercialization in the European Union and other markets recognizing the CE mark. The TMRW Vault combines digital tracking, advanced monitoring, and scalable cryostorage, modernizing fertility clinics' specimen management systems.

The TMRW Vault Freezer is designed for cryogenic storage of reproductive specimens and improves identification and traceability. The accompanying Workstation aids in sample transfer and order management through a software interface. The system provides onsite digital specimen management, continuous monitoring, and scalable storage, addressing the shortcomings of traditional manual systems.

This development follows Reprotech's merger with TMRW Life Sciences and acquisition of IMT Matcher, creating a comprehensive solution for fertility clinics.