The European Medical Device Regulation (MDR)
EU Regulation 2017/745, known as the Medical Device Regulation (MDR), has introduced significant changes to the rules on the production and marketing of medical devices in the European Union.
EU Regulation 2017/745, known as the Medical Device Regulation (MDR), has introduced significant changes to the rules on the production and marketing of medical devices in the European Union.
Bericah S.p.A., a leading company in the field of Medical Devices and Disposable Personal Protective Equipment, is pleased to announce the release of the General Catalog for the Professional – Retail – Food sectors.
We are pleased to announce the release of our new corporate website, designed to provide a better online experience for our customers.
Bericah S.p.A. is a company specialized in the production and distribution of disposable devices for crucial sectors such as the medical, professional, and organized retail (GDO) industries.
EU Regulation 2017/745, known as the Medical Device Regulation (MDR), has introduced significant changes to the rules on the production and marketing of medical devices in the European Union.
We are pleased to announce the launch of our new company website, designed to provide a better online experience for our customers.
Bericah S.p.A. is a company specialized in the production and distribution of disposable devices for crucial sectors such as the medical, professional, and organized retail (GDO) industries.