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OSARTIS GmbH

Manufacturer of medical devices registered in the European database in Münster, Germany.

Registration number (SRN)DE-MF-000009545
Short nameOSARTIS
RoleManufacturer
StatusActive
CountryGermany
City64839 Münster
AddressAuf der Beune, 101 64839 Münster
Registered on2021-07-12

United States market access

FDA establishment register Registered with the U.S. FDA
Matched entryOSARTIS GMBH (DE) · FDA 9615014

Notified body certificates

CertificateStatusExpiryTypeBody
G70 107266 0014valid2028-06-19Technical documentationNB 0123
G15 107266 0028valid2028-04-26Quality management systemNB 0123

⚠️ 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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