Clarification regarding press release about CE marking

With reference to yesterday’s press release, where we informed that we have filed TK 210 ELISA for CE mark registration at the Medical Products Agency (LMV), we would like to make a clarification. LMV does not approve products for CE mark but register the manufacturer and product as filed for CE marking. The product can then be marketed as CE marked. The processing time for this registration by LMV is usually 2-3 weeks.

For additional information please contact:

Jan Stålemark, CEO
AroCell AB (publ)
Tel: +46 706 926206

For press release in Swedish, PDF