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Registry EUDAMED 30 FDA 510(k) incl. De Novo FDA PMA GUDID

Country / market European Union (all) 30

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Germany 30

Risk class Class I Class IIa 30 Class IIb Class III 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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30 devices foundsorted by relevance

Manufacturer: RECK-Technik GmbH & Co. KG× Clear all

DeviceDevice · Manufacturer · Authorizations Verified

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MOTOmed muvi

RECK-Technik GmbH & Co. KG,Germany

Active Regimes: CE MDR Registry: EUDAMED Class:IIa
MOTOmed layson

RECK-Technik GmbH & Co. KG,Germany Group of variants

Active Regimes: CE MDR Registry: EUDAMED Class:IIa
MOTOmed loop

RECK-Technik GmbH & Co. KG,Germany Group of variants

Active Regimes: CE MDR Registry: EUDAMED Class:IIa

Showing 21-30 of 30

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