ZOLL AED Plus defibrillator approved under EU MDR

Zoll has announced that its ZOLL AED Plus defibrillator has secured approval under the European Union Medical Device Regulation 2017/745, commonly referred to as EU MDR.

EU MDR is the European Union Medical Device Regulation 2017/745 that was adopted in 2017 by the European Parliament and the Council of the European Union. It governs the clinical investigation, production and distribution of medical devices in Europe, ensuring a high standard of safety and quality.

ZOLL now has CE marking for the ZOLL AED Plus defibrillator under the EU MDR.

“ZOLL is happy to have received our second MDR certification for our AED Plus. With this new certification, ZOLL customers will know that this device has passed the most stringent level of European medical regulation for a medical device.”

Elijah White, President of ZOLL’s Acute Care Technology division.

ZOLL says it is now continuing to work diligently towards achieving EU MDR approval for its Powerheart G5 and certification for ZOLL’s full portfolio of products.

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