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Results for “Single Use Guide Sheath Kit”

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Registry EUDAMED 43 FDA 510(k) 2 FDA PMA GUDID 6

Country / market European Union (all) 43 United States 8

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Germany 43

Risk class Class I Class IIa 43 Class IIb Class III Class II (US) 8

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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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51 devices foundsorted by relevance

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Registry

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Single Use Guide Sheath Kit

Alton (Shanghai) Medical Instruments Co., Ltd.,China

Active Regimes: CE MDR Registry: EUDAMED Class:IIa
Single Use Guide Sheath Kit K-401

Olympus Medical Systems Corp.,Japan

Active Regimes: CE MDD Registry: EUDAMED Class:IIa
Single Use Guide Sheath Kit K-403

Olympus Medical Systems Corp.,Japan

Active Regimes: CE MDD Registry: EUDAMED Class:IIa

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