IMPORTANT NEWS CONCERNING OUR CE MARKED PRODUCT RANGE

As of May 26th, 2022, the new In Vitro Diagnostic Medical Devices Regulation (IVDR) will be applicable. Following the updated product classification and requirements of the IVDR, those Diaclone products that have CE marking will be available for research and further manufacturing use without CE marking to fully comply with the new regulation.

We continuously apply the same production process and quality control methods as before, ensuring the high quality that Diaclone products are known for, and these products continue to be available without CE marking and have the same catalogue number as before.

List of products affected