CE CERTIFICATE
The EC Certificate, in accordance with Directive 93/42/EEC Annex V, signifies compliance with the essential requirements for medical devices. It is a testament to the implementation of a robust Production Quality Assurance system. This certificate holds significant importance for manufacturers as it demonstrates their commitment to ensuring the safety, performance, and quality of their medical devices. It serves as evidence that the devices meet the necessary regulatory standards and can be legally marketed and sold within the European Union.