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Results for “DK50 PLUS”

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Registry EUDAMED 35 FDA 510(k) FDA PMA GUDID

Country / market European Union (all) 35

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Slovakia 35

Risk class Class I Class IIa 35 Class IIb Class III Class II (US)

More classes (11)

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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35 devices foundsorted by relevance

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DK50 Plus S/M UDI-DI 08586014621940

EKOM spol. s r.o.,Slovakia

Active Regimes: CE MDR CE MDD Registry: EUDAMED Class:IIa
7 variants
- DK50 Plus S/M 4031020A1-403 Withdrawn
- DK50 Plus S/M 4031020A1-405 Withdrawn
- DK50 Plus S/M 4031020B1-401 Withdrawn
- DK50 Plus S/M 4031020B1-403 Withdrawn
- DK50 Plus S/M 403102051-400 Withdrawn
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DK50 Plus S UDI-DI 08586014622169

EKOM spol. s r.o.,Slovakia

Active Regimes: CE MDR CE MDD Registry: EUDAMED Class:IIa
9 variants
- DK50 Plus S 403C02001-400 Withdrawn
- DK50 Plus S 403C02001-403 Withdrawn
- DK50 Plus S 403C02001-404 Withdrawn
- DK50 Plus S 403102001-400 Withdrawn
- See all variants of this device
DK50 Plus UDI-DI 08586014622404

EKOM spol. s r.o.,Slovakia

Active Regimes: CE MDR CE MDD Registry: EUDAMED Class:IIa
10 variants
- DK50 Plus 403C01001-401
- DK50 Plus 403C01001-402 Withdrawn
- DK50 Plus 403101005-405
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DK50 Plus/M UDI-DI 08586014622008

EKOM spol. s r.o.,Slovakia

Active Regimes: CE MDR CE MDD Registry: EUDAMED Class:IIa
9 variants
- DK50 Plus/M 4031010A1-403 Withdrawn
- DK50 Plus/M 4031010B1-402
- DK50 Plus/M 4031010B1-404 Withdrawn
- DK50 Plus/M 403101051-400
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