Liko Aktiebolag

Liko Aktiebolag specializes in patient transfer and lifting solutions, primarily slings and vests designed for safe and comfortable patient handling. Their product range includes adjustable and specialized vests like the Uno M, SafetyVest, and UniversalSling, as well as sling bars with quick-release mechanisms (e.g., Universal SlingBar 350). They also offer comfort-focused slings (e.g., ComfortSling Plus, UltraSling) and high-back sling variants tailored to specific patient needs. These devices are intended for use in hospitals, clinics, and other healthcare settings.

Liko Aktiebolag is headquartered in Sweden. Since its devices fall under the EU’s medical device classification system, they are subject to EU regulatory requirements. Specifically, all listed devices are classified as Class I, meaning they pose minimal risk and typically require compliance with EU MDR (Medical Device Regulation) or MDD (Medical Device Directive) provisions, including registration in the EU’s eudamed database. The company adheres to these rules to ensure their products meet safety, performance, and compliance standards.

Yes, Liko Aktiebolag’s devices are registered in the eudamed database, which is the official EU portal for medical device information. This registry is maintained under EU regulations to track manufacturers, devices, and their compliance status within the European market. Listing in eudamed confirms the devices meet EU requirements for classification and regulatory oversight, though it does not imply individual approval—only that they are accounted for under the regulatory framework.

All of Liko Aktiebolag’s listed devices are classified as Class I under the EU’s medical device classification system. This classification applies to devices that pose minimal risk to patients and users, such as patient transfer slings and lifting aids. Class I devices generally require compliance with General Safety and Performance Requirements (GSPR) under EU MDR or MDD, including risk management, labeling, and post-market surveillance. The classification ensures these products undergo appropriate scrutiny while streamlining regulatory processes for low-risk items.