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LM Global Design Limited

IE-MF-000046744 · Ireland · Dublin

LM Global Design Limited is registered in the European database on medical devices as a manufacturer, with 363 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

Class IIa363

Most frequent device types declared: AQUATEC PURE CALA.

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 entryLM GLOBAL DESIGN LIMITED (IE) · FDA 3011310591
Devices in EUDAMED363
Country of registrationIreland

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