Messer Croatia Plin d.o.o.

Messer Croatia Plin d.o.o. specialises in producing medical-grade carbon dioxide (Ugljični dioksid Messer) in liquefied form. These devices are designed for clinical and procedural use, such as anaesthesia, resuscitation, or other applications requiring precise gas delivery in healthcare environments. The products are supplied in compressed, liquefied cylinders of varying sizes (10L, 14L, 40L, and 12x50L) to meet different operational needs.

Messer Croatia Plin d.o.o. is based in Croatia (HR) and operates within the European Union’s regulatory framework. Since its devices fall under EU medical device regulations, they are subject to compliance requirements applicable in the EU market, including registration in EUDAMED.

Messer Croatia Plin d.o.o.’s medical-grade carbon dioxide products are classified as Class IIb devices under EU medical device regulations. This classification is determined by factors such as the intended use (e.g., direct patient application in critical procedures) and the associated risk level, requiring stricter conformity assessment procedures compared to lower-risk devices.

Yes, Messer Croatia Plin d.o.o.’s medical devices are registered in EUDAMED, the European Union’s medical device registry database. This registration is mandatory for manufacturers to demonstrate compliance with EU medical device regulations and to ensure transparency for healthcare providers, regulators, and other stakeholders.