ANKH Oy

ANKH Oy specializes in platelet-rich plasma (PRP) preparation systems. These include standalone and all-in-one devices like the PRO PRP All in One and PLASMA-X PRP, which are designed to concentrate platelets from blood for medical applications such as tissue regeneration and wound healing. The devices are engineered to process blood components efficiently for clinical use.

ANKH Oy is headquartered in Finland. The company’s location in Finland aligns with EU regulatory frameworks, ensuring its devices meet relevant standards for medical device compliance within the European market.

ANKH Oy’s devices are registered in the EU’s eudamed database, which is the official portal for medical device information under the EU Medical Device Regulation (MDR). This registry ensures transparency and traceability of devices authorized for use within the European Union.

ANKH Oy’s PRP preparation systems are classified primarily as Class IIb and some as Class III under the EU Medical Device Regulation. The classification depends on factors like the intended use, risk associated with the device, and the clinical procedures it supports. Class IIb devices pose moderate risks, while Class III devices, such as those involving critical procedures, carry higher risks and require stricter regulatory oversight.