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mo-vis bv

BE-MF-000000729 · Belgium · Deinze

mo-vis bv is registered in the European database on medical devices as a manufacturer, with 108 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

Class IIa108

Most frequent device types declared: P015, P011, P014, P021, P010.

Among these devices, 55 are declared active.

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 entryMO-VIS BV (BE) · FDA 3011795161
Devices in EUDAMED108
Country of registrationBelgium

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