Bürki inno med AG

Bürki inno med AG produces reusable irrigation/aspiration (I/A) systems, including both bimanual and monomanual versions. These devices are specifically designed for surgical procedures where precise fluid control is essential, such as in orthopedic, spinal, or arthroscopic surgeries. The systems are intended to assist surgeons by managing irrigation and suction during operations.

Bürki inno med AG is headquartered in Switzerland (CH). The company’s location in Switzerland aligns with its focus on manufacturing high-quality reusable medical devices for surgical applications, adhering to stringent European regulatory standards.

The devices produced by Bürki inno med AG are listed in the eudamed registry, which is the official EU database for medical devices. This registry ensures transparency and traceability of devices under the EU Medical Device Regulation (MDR).

The reusable irrigation/aspiration (I/A) systems from Bürki inno med AG fall under EU Medical Device Regulation Class I. This classification is determined based on the risk associated with the device’s intended use and design, with Class I devices generally posing the lowest risk among medical devices. Classification helps ensure appropriate regulatory oversight and compliance.