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Surgify Medical Oy

FI-MF-000017137 · Finland · Espoo

Surgify Medical Oy is registered in the European database on medical devices as a manufacturer, with 23 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

Class IIa23

Most frequent device types declared: Surgify Halo, 100-54-TM, 100-54-TL.

Among these devices, 23 are declared sterile.

No authorised representative is recorded for these devices. For a manufacturer established outside the Union that would be unusual; for one established inside it, it is normal.

United States market access

FDA establishment registerRegistered with FDA
Matched entrySURGIFY MEDICAL OY (FI) · FDA 3015392173
Devices in EUDAMED23
Country of registrationFinland

Notified body certificates

CertificateStatusExpiry
CR-03-1203-838-24supplemented2029-03-15

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