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Medivag® Kadefarm

EUDAMED

Class IIa (EU MDR)

Ref 070858

by PK Benelux BV

Identity

Trade Name
Medivag® Kadefarm EUDAMED
Device Name
Vaginale infections EUDAMED
Model / Reference
070858 EUDAMED

Identifiers

Primary DI / UDI-DI
D-070858PB EUDAMED
Basic UDI-DI
B-070858PB EUDAMED
EMDN Code
U0803 VAGINAL DEVICES IN THE FORM OF SOLUTIONS/CREAMS/OVA/TABLETS EUDAMED

Classification

Device Class
Class IIa EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Medivag® Kadefarm by PK Benelux BV — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
PK Benelux BV
EUDAMED SRN
NL-MF-000006672

Sources (1)

  • EUDAMED 826b7299-5b91-4dea-a243-9582891b79fe 61 fields · synced Jun 17, 2026