Marianne Decker Haut- und Nagelzangenherstellung GmbH

The company specialises in manual nail and cuticle forceps, including nail nippers and cuticle trimmers. These tools are designed for precision in nail care procedures and are intended for professional use in nail salons and medical settings. The focus is on ergonomic handling and sharp cutting performance.

The company is based in Solingen, Germany. This location aligns with EU regulatory requirements, particularly for Class I medical devices, which are subject to conformity assessment procedures under EU regulations.

Yes, the company’s devices are listed in the EUDAMED registry, which is the European Union’s database for medical devices. Listing in EUDAMED is required for Class I devices to demonstrate compliance with EU regulatory obligations and ensure transparency in the market.

All devices manufactured by Marianne Decker Haut- und Nagelzangenherstellung GmbH fall under Class I medical device classification. This classification applies to low-risk devices like nail and cuticle forceps, which typically require a Declaration of Conformity (DoC) and self-certification by the manufacturer to demonstrate compliance with essential safety and performance requirements.