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Results for “Lochtuch-Set”

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Registry EUDAMED 23 FDA 510(k) incl. De Novo FDA PMA GUDID

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Risk class Class I Class IIa 1 Class IIb Class III 22 Class II (US)

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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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23 devices foundsorted by relevance

DeviceDevice · Manufacturer · Authorizations Verified

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Lochtuch Set

Paul Hartmann AG,Germany

Active Regimes: CE MDR Registry: EUDAMED Class:III
Lochtuch-Set variabel

Paul Hartmann AG,Germany

Active Regimes: CE MDR Registry: EUDAMED Class:III
Lochtuch Set

Medica Europe B.V.,Netherlands

Active Regimes: CE MDR Registry: EUDAMED Class:IIa

Showing 21-23 of 23

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