Results for “Occlutech Paravalvular Leak Device Procedure Pack”

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Registry EUDAMED 59 FDA 510(k) incl. De Novo FDA PMA GUDID

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Occlutech Paravalvular Leak Device Procedure Pack

Occlutech GmbH,Germany Group of variants

Active Regimes: CE MDR Registry: EUDAMED Class:III
Occlutech Paravalvular Leak Device Procedure Pack

Occlutech International AB,Sweden Group of variants

Active Regimes: CE MDR Registry: EUDAMED Class:III

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