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Results for “SENSATION™”

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Registry EUDAMED 703 FDA 510(k) incl. De Novo 17 FDA PMA GUDID 222

Country / market European Union (all) 696 United States 239

More countries (11)

Netherlands 434 France 231 Italy 11 Poland 9 Spain 4 Northern Ireland 4 Germany 3 Greece 1 Ireland 1 Portugal 1 Romania 1

Risk class Class I 794 Class IIa 8 Class IIb 34 Class III 1 Class II (US) 96

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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933 devices foundsorted by relevance

DeviceDevice · Manufacturer · Authorizations Verified

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Registry

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K2 Sensation® with D/P Flexion

Össur Iceland ehf.,Iceland Group of variants

Active Regimes: CE MDR Registry: EUDAMED Class:I
K2 Sensation®

Össur Iceland ehf.,Iceland Group of variants

Active Regimes: CE MDR Registry: EUDAMED Class:I
Fiesta Sensation

Innolatex Sdn. Bhd.,Malaysia

Active Regimes: CE MDR Registry: EUDAMED Class:IIb

Showing 321-340 of 933

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