Steripette now registered as Medical Device Class Is according to MDR
The Steripette – our long-established capillary pipette for assisted reproduction, trusted by embryologists worldwide – is now officially approved as a Class Is medical device under the EU Medical Device Regulation 2017/745 (MDR). With this certification, the Steripette carries the CE mark and is approved for distribution throughout the European Economic Area (EEA).
For you as a user, nothing changes in practice – except the added reassurance of working with an MDR compliant, CE-marked product. The Steripette remains what it has always been: a trusted, safe, and practical tool fulfilling the highest standards for reproductive medicine.
Proven quality, now fully compliant with MDR standards
For many years, the Steripette has been a reliable choice in ART laboratories, valued for easy and safe handling of oocytes and embryos. Our handling capillary is individually packed, sterile and tested for embryotoxicity, endotoxins and bioburden, ensuring the highest level of safety in sensitive ART applications. With MDR approval, its quality and safety are now officially recognized under the strict European regulatory framework.Your benefits at a glance
- Regulatory assurance: MDR Class Is approval stands for a safe product with optimum performance according to the latest standards
- Reliable sterility: Supplied sterile for maximum safety for sensitive ART procedures
- Trusted performance: Enjoy the same user-friendliness the Steripette has always offered with no changes in handling or application
- Future-proof availability: MDR conformity ensures long-term distribution throughout the EEA
For you as a user, nothing changes in practice – except the added reassurance of working with an MDR compliant, CE-marked product. The Steripette remains what it has always been: a trusted, safe, and practical tool fulfilling the highest standards for reproductive medicine.
