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CellaVision AB

SE-MF-000002377 · Sweden · Lund

CellaVision AB is registered in the European database on medical devices as a manufacturer, with 48 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

other48

Most frequent device types declared: CellaVision® Bone Marrow Aspirate Application.

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 entryCELLAVISION AB (SE) · FDA 3003630693
Devices in EUDAMED48
Country of registrationSweden

Other manufacturers in Sweden

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