If a certificate is missing or invalid, it must be requested directly from the manufacturer.
The date the documents were recorded, likely to comply with device registration or market surveillance requirements. 2. How to Open and Review the File URPL DoC, 03.01.2023.zip
The Polish regulatory body responsible for medical devices. If a certificate is missing or invalid, it
A manufacturer's declaration that a device meets all applicable regulatory requirements (e.g., MDR 2017/745 in the EU). MDR 2017/745 in the EU).