IRVINE, CA, and HERSTAL, BELGIUM - 07:00 CEST, June 08, 2017 - MDxHealth SA (Euronext:MDXH.BR) today announced the launch in Europe and other markets* of the SelectMDx ® for Prostate Cancer in vitro ...
The DNA/RNA Shield ™ product line includes sample collection, preservation, and transportation devices for medical specimens used in research and are now available for in vitro diagnostics (e.g., ...
SALT LAKE CITY--(BUSINESS WIRE)--Spectrum Solutions, LLC today announced receiving CE Mark approval for the sale and distribution of its groundbreaking SDNA saliva collection device for IVD molecular ...
PRNewswire/ -- Seegene Inc. (KQ 096530), South Korea's leading molecular diagnostics company, announced on August 20 that it has obtained CE marking for the use of Combo Swab, a self-collection device ...
Swiss data company Sophia Genetics has secured a CE mark for its genomic analysis platform under the EU’s revised In Vitro Diagnostics Regulation (IVDR). The IVDR CE mark certifies that the company’s ...
PreciPoint, a German digital microscopy company specializing in digital microscopes and digital pathology solutions, today announced the market launch of its iO:M8 Digital Live Microscope. The ...
Today, Roche announced the launch of its new CE certified IVD version of the MagNA Pure 96 System for automated sample preparation. By providing a maximum of lot-to-lot consistency and highest quality ...
Tampa, FL, Jan. 31, 2018 (GLOBE NEWSWIRE) -- Cancer informatics and digital pathology workflow solution provider Inspirata ®, Inc. announced today that it has acquired Pittsburgh, PA-based Omnyx from ...
YONGIN, South Korea, Sept. 1, 2022 /PRNewswire/ -- Noul Co., Ltd., (376930.KR), a KOSDAQ-listed biotech startup, has obtained CE-IVD marks for two of its products. Based on this mark, Noul plans to ...
New Delhi [India], October 24: Indian IVD manufacturers face growing regulatory hurdles under the EU IVDR. I3CGLOBAL provides strategic CE Marking support to small, medium, and large-scale ...
Professional services consultancy, Procorre is urging the Medical Devices industry to take action ahead of the new ISO13485:2016 International Standard and MDD & IVD ‘Recast’ which become mandatory in ...
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