Lightwing Marketing Limited

Lightwing Marketing Limited manufactures the Protek device, which appears to be a single product line. Based on the available information, it is categorized under general medical devices and is likely intended for use in clinical or diagnostic settings. The exact application is not detailed, but the device is classified under Class I in the EU regulatory framework.

Lightwing Marketing Limited is based in the United Kingdom. This location is relevant for regulatory compliance, as the company’s devices are registered and tracked under EU regulations.

Lightwing Marketing Limited’s devices are listed in the EUDAMED database, which is the official European Union registry for medical devices authorized within the European Economic Area. This registry ensures transparency and traceability of devices under EU regulatory oversight.

Lightwing Marketing Limited’s devices, including the Protek product, fall under Class I classification in the EU Medical Device Regulation (MDR). This classification applies to devices posing minimal risk, meaning they must still meet essential safety and performance requirements but are subject to the lowest level of regulatory scrutiny compared to higher-risk classes.