TÜV SÜD partners with DBG TetraKom for Exclusive
Regulatory Webinar for MedTech Professionals

On dd.mm.2026, 00:00 h – 00:00 h

Device Classification - Pittfalls, Claims & Intended Purpose

presented by

Jan Herzer

TÜV SÜD Product Specialist and Manager of CE certifications

Why Should You Attend This Webinar!

  • Explore practical examples and actionable approaches to accurate device classification
  • Learn how to define a clear and compliant Intended Purpose statement
  • Avoid common classification pitfalls and incorrect claims that can delay approval
  • Participate in a live Q&A session to get answers to your specific questions
  • Connect and interact with a focused community of regulatory professionals

Who is it for!

MedTech Entrepreneurs, Consultants, Regulatory Professtionals

Join our Upcoming Webinar!

Please fill out the following form completely.

Once you’ve successfully registered, you’ll receive a confirmation email with all the information you need to participate, including your personal access link.

Registration Form