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Registry EUDAMED 331 FDA 510(k) incl. De Novo 28 FDA PMA GUDID

Country / market European Union (all) 311 United States 28

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Belgium 310 Italy 1

Risk class Class I Class IIa 93 Class IIb Class III 238 Class II (US) 28

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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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359 devices foundsorted by relevance

Manufacturer: Terumo Europe N.V.× Clear all

DeviceDevice · Manufacturer · Authorizations Verified

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Ultimaster Tansei

Terumo Europe N.V.,Belgium Group of variants

Active Regimes: CE MDR Registry: EUDAMED Class:III
Ultimaster Nagomi

Terumo Europe N.V.,Belgium

Expiring Regimes: CE MDR Registry: EUDAMED Class:III
RADIFOCUS Guide Wire M Non-Vascular

Terumo Europe N.V.,Belgium

Active Regimes: CE MDR Registry: EUDAMED Class:IIa

Showing 301-320 of 359

deviCERTS Global Medical Device Regulatory Database

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