European
Compliance Platform
European
Compliance Platform
11 of the 53 Notified Bodies designated under MDR or IVDR are based in Italy (NANDO, 12 October 2026): 11 under MDR, 2 under IVDR. The list below shows each one with its NB number.
| NB number | Notified Body | MDR | IVDR |
|---|---|---|---|
| 0051 | IMQ ISTITUTO ITALIANO DEL MARCHIO DI QUALITÀ S.P.A. | ✓ | ✓ |
| 0068 | MTIC InterCert S.r.l. | ✓ | – |
| 0373 | ISTITUTO SUPERIORE DI SANITA' | ✓ | ✓ |
| 0425 | ICIM S.P.A. | ✓ | – |
| 0426 | ITALCERT SRL | ✓ | – |
| 0476 | KIWA CERMET ITALIA S.P.A. | ✓ | – |
| 0477 | Eurofins Product Testing Italy S.r.l. | ✓ | – |
| 0546 | CERTIQUALITY S.r.l. | ✓ | – |
| 1282 | ENTE CERTIFICAZIONE MACCHINE SRL | ✓ | – |
| 1370 | BUREAU VERITAS ITALIA S.P.A. | ✓ | – |
| 1936 | TUV Rheinland Italia SRL | ✓ | – |
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 Italy 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.
11 with an active MDR or IVDR designation in NANDO on 12 October 2026: 11 under MDR and 2 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.