For IFU, MSDS, CoA, Batch Certificate and others, please do not hesitate to contact our team of experts, using the contact information below. customized blood typing
Certified DIN EN ISO 13485:2012
Reagents are manufactured at our own facility and are certified and licensed with complete donor traceability and safety documents. All are 100% inspected for visual clarity and color. All products manufactured and distributed are CE conform according to the European Directive 98/79/EC on in-vitro diagnostics medical devices. All manufacturing processes fully comply with the requirements of GMP.
CE-ID has a long record of experience. Already in 1996, we built up first quality management according to DIN EN ISO 9001. In order to stay up to date, we implemented the Quality Management System according to DIN EN ISO 13485 in its work processes already in 2003.