Tüv Süd (Germany)

Updated August 13, 2026

Tüv Süd (Germany) is a conformity assessment body based in Germany, identified as notified body NB 0123. NANDO lists it as currently designated under the EU Medical Devices Regulation (MDR) and the In Vitro Diagnostic Medical Devices Regulation (IVDR). Its detailed NANDO scope shows the device categories and conformity assessment activities covered by that designation.

2 Reviews

3.0 Bad · 2 reviews
Read all reviews
Overall experience
3.0
Well-organized / responsive
3.0
Regulatory pragmatism
4.0
Technical competence
3.0
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March 04, 2022

Review by company with 10-49 people

QMS audit done
Techdoc audit done
Overall experience
Well-organized / responsive
Regulatory pragmatism
Technical competence
Wait time before QMS audit
6 Months
Wait time before Techdoc audit
3 Months
Wait time before QMS certificate
4 Months
Wait time before Techdoc certificate
6 Months
Approx. cost (EUR)
26,999 €
The auditor changed so many times, prolonging processes. Different classification during this process for our products. Different time scales from different auditors. Billing with part bills that did not need to be paid.

Additional Comments (Duration/Cost): TÜV Prüfhaus was a life saver for our company. Auditor changed 3 times during initial processes.

Yes, I would choose this notified body again.

March 03, 2022

Review by company with 10-49 people

QMS audit done
Techdoc audit done
Overall experience
Well-organized / responsive
Regulatory pragmatism
Technical competence
Wait time before QMS audit
9 Months
Wait time before Techdoc audit
5 Months
Wait time before QMS certificate
6 Months
Wait time before Techdoc certificate
0 Months
Approx. cost (EUR)
20,660 €
Yes, I would choose this notified body again.

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