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).
- Sil-Select StockTM
- Sil-Select PlusTM
- GAINTM medium
As summarized in a 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
- Specific changes for Sil-Select StockTM and Sil-Select PlusTM:
- Sperm survival test (SST) is replaced by a human sperm survival assay (HSSA). This means no change in test method, but only a minor difference in calculation of results
- Viscosity is omitted as specification
- Specific changes for GAINTM medium
- Additional product specification: human sperm survival assay(HSSA) (% motility compared with control after 24 hours exposure to test medium): ≥80%
- Intended use does no longer include swim-up or density gradient preparation
If additional information is required or additional registration actions in your jurisdiction(s), please send your question to ra@fertipro.com.