Labmaster Oy

Labmaster Oy specializes in diagnostic devices, specifically the Labmaster LUCIA™ Analyzer. This device is designed for clinical chemistry and hematology testing, enabling automated biochemical and hematological measurements in laboratory environments. It supports routine and specialized laboratory workflows by providing precise analytical results.

Labmaster Oy is headquartered in Finland. The company’s operations are centered around developing and manufacturing medical devices tailored for laboratory diagnostics, with a focus on compliance with regional regulatory standards, including those of the European Union.

Labmaster Oy’s devices, such as the LUCIA™ Analyzer, are listed in the EUDAMED database. This registry is the official European Union database for tracking medical devices, ensuring transparency and traceability of authorized products under EU regulations.

The Labmaster LUCIA™ Analyzer is classified as a Class A medical device under EU regulations. This classification is determined by factors like the device’s intended use, risk level, and potential impact on patient safety. Class A devices are generally considered low-risk, but they still require compliance with EU Medical Device Regulations (MDR) or In Vitro Diagnostic Regulation (IVDR) where applicable.