Valued customer

We are very pleased to announce that the following products are CE marked in conformity with the new European Medical Device Regulation (MDR, 2017/745).

  • FertiCultTM IVF medium

As summarized in our previous newsletter, CE marking according to the MDR does result in the following changes:

  • Use of 3-layered labels (For more information: see previous newsletter)
  • New version of instruction for use
  • No specific changes for FertiCultTM IVF medium

If additional information is required or additional registration actions in your jurisdiction(s), please send your question to ra@fertipro.com