The syringe plungers are classified as accessories for medical devices, as such, they must meet the requirements of the CE marking. This marking certifies that the manufacturer meets the essential requirements for marketing and use in the European Union. In 2006, the company’s quality system obtained the ISO 9001 certification (Certificate TUV N. 50 100 5852). Accurate quality controls are performed in all stages of the production cycle, from the receipt of the raw materials until shipment to the Customer.
EU e-Privacy Directive