European
Compliance Platform
European
Compliance Platform
10 of the 53 Notified Bodies designated under MDR or IVDR are based in Germany (NANDO, 12 October 2026): 10 under MDR, 4 under IVDR. The list below shows each one with its NB number.
| NB number | Notified Body | MDR | IVDR |
|---|---|---|---|
| 0044 | TÜV NORD CERT GmbH | ✓ | – |
| 0123 | TÜV SÜD Product Service GmbH | ✓ | ✓ |
| 0124 | DEKRA Certification GmbH | ✓ | ✓ |
| 0197 | TÜV Rheinland LGA Products GmbH | ✓ | ✓ |
| 0297 | DQS Medizinprodukte GmbH | ✓ | – |
| 0482 | DNV MEDCERT GmbH | ✓ | – |
| 0483 | mdc medical device certification GmbH | ✓ | ✓ |
| 0494 | SLG PRÜF UND ZERTIFIZIERUNGS GMBH | ✓ | – |
| 0633 | Berlin Cert GmbH | ✓ | – |
| 2975 | SZUTEST Konformitätsbewertungsstelle GmbH | ✓ | – |
Source: NANDO, European Commission, 12 October 2026. Designations change: open NANDO for each body’s current scope, conditions and notification documents.
Found Notified Bodies that fit?
Describe your device once and send one request to several Notified Bodies, free. You choose the bodies; we email you when they reply.
Send my request free →Not for market access: a certificate from any Notified Body designated under MDR or IVDR is valid in the whole EU and EEA. Manufacturers pick a body in Germany for practical reasons: audit language, travel time for on-site QMS audits, and familiarity with the local market. What matters more is whether the body covers your device codes and has capacity.
10 with an active MDR or IVDR designation in NANDO on 12 October 2026: 10 under MDR and 4 under IVDR.
No. A CE certificate from any Notified Body designated under the relevant Regulation is valid across the EU and EEA.
NANDO does not show capacity. Ask each body in writing about your exact device type, the evidence it needs and its current lead times, or send one request to several bodies at once through eucertify.com.