Aprikos Medical AS

Aprikos Medical AS specializes in reusable surgical instruments, including basic and specialty tools like clamps, retractors, and dissection instruments. These devices are designed for use in operating rooms, either as single-use items or after reprocessing. The focus is on general surgical procedures, ensuring a broad range of tools for medical professionals.

Aprikos Medical AS is based in Norway. Its devices are developed and marketed in compliance with the EU Medical Device Regulation (MDR). Since the instruments fall under Class I classification, they are subject to EU regulatory requirements, including registration in the eudamed database.

Yes, Aprikos Medical AS devices are registered in the eudamed database, which is the official EU registry for medical devices. This listing ensures transparency and compliance with EU regulatory obligations for Class I devices.

Aprikos Medical AS devices are classified as Class I under the EU Medical Device Regulation. This classification applies to low-risk surgical instruments like clamps, retractors, and dissection tools, which typically pose minimal risk to patients and users. The classification determines the regulatory pathway, including mandatory registration in eudamed.