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PreventID® Vital-D

EUDAMED

Class A (EU MDR)

Ref KST80100EP

by Immundiagnostik AG

Identity

Trade Name
PreventID® Vital-D EUDAMED
Device Name
DrySpot EUDAMED
Model / Reference
KST80100EP EUDAMED

Identifiers

Primary DI / UDI-DI
04050598009592 EUDAMED
Basic UDI-DI
4050598DVDrySpotPL EUDAMED
Direct Marketing DI
04050598009592 EUDAMED
EMDN Code
A99 DEVICES FOR ADMINISTRATION, WITHDRAWAL AND COLLECTION - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

PreventID® Vital-D by Immundiagnostik AG — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

Manufacturer
Immundiagnostik AG
EUDAMED SRN
DE-MF-000020905

Sources (1)

  • EUDAMED d4cf43b7-79a8-4d12-a13f-d84e8d59ba43 61 fields · synced Jun 18, 2026