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Results for “Single Use Preloaded Sphincterotome V(Distal Wireguided) KD-VC631Q-07203S”

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Registry EUDAMED 1 FDA 510(k) incl. De Novo FDA PMA GUDID 3

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Risk class Class I Class IIa Class IIb Class III Class II (US) 3

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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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3 devices foundsorted by relevance

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Single Use Preloaded Sphincterotome V(Distal Wireguided) KD-VC631Q-07203S

Olympus Medical Systems Corporation,FDA registration: Japan

Active Regimes: CE MDD Registry: EUDAMEDGUDID Class:II
Single Use Preloaded Sphincterotome V(Distal Wireguided) KD-VC631Q-07203S

Olympus Medical Systems Corporation,FDA registration: Japan Group of variants

None Registry: GUDID Class:II

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