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ExiStation™ FA DNA/RNA Kit (V3)

EUDAMED

Class A (EU MDR)

Ref K-4815

by BIONEER Corporation

Identity

Trade Name
ExiStation™ FA DNA/RNA Kit (V3) EUDAMED
Device Name
ExiStation™ FA DNA/RNA Kit (V3) EUDAMED
Model / Reference
K-4815 EUDAMED

Identifiers

Primary DI / UDI-DI
08809537078733 EUDAMED
Basic UDI-DI
880935717K4815BP EUDAMED
EMDN Code
W0105900101 REAGENTS FOR DNA AND/OR RNA EXTRACTION AND PREPARATION: BACTERIA AND/OR VIRUS 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

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Category: Nucleic acid extraction/isolation kit IVD

ExiStation™ FA DNA/RNA Kit (V3) by Bioneer Corporation — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Nucleic acid extraction/isolation kit IVD.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

Manufacturer
BIONEER Corporation
EUDAMED SRN
KR-MF-000018672
Authorised Representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Sources (1)

  • EUDAMED 6ea90b0f-7e63-4c4e-8234-e83641aed3e2 61 fields · synced Jul 17, 2026