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Results for “Maxi Move”

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Registry EUDAMED 523 FDA 510(k) incl. De Novo FDA PMA GUDID 33

Country / market European Union (all) 474 United States 33

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Austria 56 Germany 48 Portugal 42 Denmark 39 Northern Ireland 36 Greece 28 Hungary 26 Estonia 24 Lithuania 24 Romania 24 Slovenia 24 Slovakia 22 Spain 20 Czechia 18 Poland 16 Belgium 14 Netherlands 11 Norway 11

Risk class Class I 546 Class IIa Class IIb Class III Class II (US)

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Class A Class B Class C Class D IVD General IVD Annex II List A IVD Annex II List B IVD for self-testing Active implantable (AIMDD) Unclassified (FDA) Not classified (FDA)

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546 devices foundsorted by relevance

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Maxi Move

Arjohuntleigh AB,Sweden Group of variants

Withdrawn Regimes: CE MDR, withdrawn Registry: EUDAMED Class:I
Maxi Move 5

Arjohuntleigh AB,Sweden Group of variants

Active Regimes: CE MDR Registry: EUDAMED Class:I
Mover - FLEXI - MAXI

Koval Proizvodnja In Trgovina, D.O.O.,Slovenia

Active Regimes: CE MDR Registry: EUDAMED Class:I

Showing 461-480 of 546

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