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ASSUT EUROPE SPA

Manufacturer of medical devices registered in the European database in Rome, Italy.

Registration number (SRN)IT-MF-000018178
Short nameAssut
RoleManufacturer
StatusActive
CountryItaly
City00173 Rome
AddressG. Gregoraci, 12 00173 Rome
Registered on2021-12-17

United States market access

FDA establishment register Similar name in the FDA register — unverified
Matched entryAssut Europe S.P.A. (IT) · FDA 9617547

⚠️ A similar name exists. We do not assert it is the same company — a name alone is not proof. This one needs a human check.

Notified body certificates

CertificateStatusExpiryTypeBody
CVD0060260126valid2028-08-07Technical documentationNB 0373
CVD0051260326supplemented2028-08-07Technical documentationNB 0373
CVD0050250126supplemented2028-08-07Technical documentationNB 0373
CVD0049250126supplemented2028-08-07Technical documentationNB 0373
CVD0048250326supplemented2028-08-07Technical documentationNB 0373
CVD004725valid2028-08-07Technical documentationNB 0373
CVD0044250226supplemented2028-08-07Technical documentationNB 0373
CVD0041240324supplemented2028-08-07Technical documentationNB 0373
CVD0040240325supplemented2028-08-07Technical documentationNB 0373
CVD003924valid2028-08-07Technical documentationNB 0373
CVD003624valid2028-08-07Technical documentationNB 0373
CVD0035241125supplemented2028-08-07Technical documentationNB 0373
CVD0034240124supplemented2028-08-07Technical documentationNB 0373
CVD0033240126supplemented2028-08-07Technical documentationNB 0373
CVD0032240124supplemented2028-08-07Technical documentationNB 0373
CVD0031240425supplemented2028-08-07Technical documentationNB 0373
CVD0030240124supplemented2028-08-07Technical documentationNB 0373
CVD002023valid2028-08-07Technical documentationNB 0373
CVD0014230224supplemented2028-08-07Technical documentationNB 0373
CSQ0013236126supplemented2028-08-07Quality management systemNB 0373

⚠️ State of the register on 2026-08-20. EUDAMED shows only the current version of a certificate — earlier versions are not published, by the Commission or by anyone. A certificate shown as valid here may have changed since. For a legally binding check, consult EUDAMED directly.

The SRN is the registration number assigned by the European Commission. It has been mandatory since 28 May 2026 for any operator placing a medical device on the Union market. Contact details are published in the official register; we do not reproduce them here.

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