Seventeen categories of device information must be in the database for a UDI device, entered before the end of 30 days starting on the first supply day on or after the general start day. The categories run from the manufacturer TGA number and name to handling, warnings, instructions, single-use status, sterilisation, batch and serial flags, date flags, blood donation flag, software flag, kit flag and base package quantity. If the clinical size type is held, the value and unit must also be entered.
The graph holds this control, the 0 it maps to, and the evidence behind each claim, over MCP and REST.