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Results for “Auralis”

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Registry EUDAMED 26 FDA 510(k) incl. De Novo FDA PMA GUDID 19

Country / market European Union (all) 25 United States 19

More countries (14)

Austria 12 Italy 2 Belgium 1 Czechia 1 Estonia 1 Greece 1 Spain 1 Hungary 1 Ireland 1 Iceland 1 Poland 1 Romania 1 Slovenia 1 Slovakia 1

Risk class Class I 12 Class IIa 14 Class IIb Class III Class II (US) 11

More classes (11)

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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37 devices foundsorted by relevance

DeviceDevice · Manufacturer · Authorizations Verified

Status

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Registry

Class

Auralis 636M02S-P

Arjohuntleigh, Inc.,FDA registration: United States

None Registry: GUDID Class:II
Auralis 636003US

Arjohuntleigh, Inc.,FDA registration: United States

None Registry: GUDID Class:II
Auralis

Arjohuntleigh AB,Sweden Group of variants

Active Regimes: CE MDR Registry: EUDAMED Class:IIa
Auralis

Arjohuntleigh AB,Sweden

Active Regimes: CE MDR Registry: EUDAMED Class:I

Showing 21-37 of 37

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