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Stereotaxis receives CE mark certification for devices in Europe

Stereotaxis Inc. recently received CE mark recertification for all its devices currently available in Europe under the new Medical Device Regulation (MDR) regulatory framework. The MDR has replaced the European Medical Device Directive and includes more stringent standards but meeting the new requirements comes with frustrations and costs for many companies.

Stereotaxis Receives CE Mark Recertification Under EU's MDR Regulatory Framework

Neoss® Group receives EU Medical Device Regulation (MDR) certifications for implants and abutments

ROKIT HEALTHCARE Achieves European Certification for Cutting-Edge Organ Regeneration

Form 10-K IRADIMED CORP For: Dec 31