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Jabbla

BE-MF-000049893 · Belgium · Gent

Jabbla is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

Class IIa6

Most frequent device types declared: Tellus.

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 entryJABBLA (BE) · FDA 3007275470
Devices in EUDAMED6
Country of registrationBelgium

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