Patent Title Patent Number Patent Authority (USPTO, EPO, WIPO, IRIPO, etc.) Date of Registration Current Status (Granted, Pending, In Examination, Renewed) Link to Patent Document (optional)

Technology Field (Medical, Mechanical, Electronics, ICT, Biotechnology, Materials, etc.) Intended Application (Consumer, Industrial, Medical, Laboratory, etc.) Possible Relevant CE Directives: Medical Device Regulation (MDR) Low Voltage Directive (LVD) EMC Directive Machinery Directive Radio Equipment Directive PPE Directive RoHS Directive Other (please specify)

Detailed Description of Function Key Innovation / Novelty Components & Materials Used Product Images, Diagrams, or Schematics (File Upload) Known or Potential Risks (Risk Factors)

Idea / Concept Early Prototype Laboratory Prototype Pre-production Model Mass-produced Product Existing Test Reports (if any) Standards Already Applied (ISO, EN, ASTM, IEC…)

Has any risk analysis been performed? (Yes / No) Method Used (FMEA, HACCP, ISO 14971, or Other) Risk Assessment Documents (Upload) Identified Hazards (Mechanical, Electrical, Biological, Chemical, Thermal, etc.)

Functional Tests Needed Safety Tests EMC / Electrical Tests Biocompatibility Tests (for medical devices) Environmental / Chemical Tests Preferred Evaluation Method: Self-Declaration Notified Body Certification (please specify if known)

Production Type: In-house / Outsourced Manufacturing Country Factory Certifications (ISO 9001, ISO 13485, etc.) Material Sourcing Details Quality Control (QC) or Quality Assurance System Used

Purpose of the Evaluation: Patent Review Only CE Roadmap Consultation Full CE Certification Support Expected Timeline (Weeks / Months) Request for Expert Meeting (Yes / No)