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PreventID® Vital-D

EUDAMED

Class A (EU MDR)

Ref KST80101EP13Ref KST80100G5Ref KST80100GP

by Immundiagnostik AG

Identity

Trade Name
PreventID® Vital-D EUDAMED
Device Name
DrySpot EUDAMED
Model / Reference
KST80101EP13 EUDAMED
KST80100G5 EUDAMED
KST80100GP EUDAMED

Identifiers

Primary DI / UDI-DI
04050598014930 EUDAMED
04050598009608 EUDAMED
04050598009615 EUDAMED
Basic UDI-DI
4050598DVDrySpotPL EUDAMED
Direct Marketing DI
04050598014930 EUDAMED
04050598009608 EUDAMED
04050598009615 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 (3)

  • EUDAMED 6331f988-7a7d-42bf-bb75-0eafe90164f6 61 fields · synced Jul 27, 2026
  • EUDAMED b1c9be65-3162-4167-a0a3-b7d5a0dfb599 61 fields · synced May 17, 2026
  • EUDAMED 39b87c46-a2e9-4c0a-b5f8-5a31cc5120f9 61 fields · synced May 18, 2026