← Back to catalogue

Rapid Detection System

EUDAMED

Class A (EU MDR)

Ref DA8130Model T-elfie

by Daan Gene Co., Ltd.

Identity

Trade Name
Rapid Detection System EUDAMED
Device Name
Rapid Detection System EUDAMED
Model / Reference
T-elfie EUDAMED
DA8130 EUDAMED

Identifiers

Primary DI / UDI-DI
06928103081303 EUDAMED
Basic UDI-DI
69281030813XFZ EUDAMED
EMDN Code
W02050116 NUCLEIC ACID TESTING INTEGRATED EXTRACTION /AMPLIFICATION /DETECTION SYSTEMS EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Netherlands 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

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

No

EUDAMED

Category: Nucleic acid sample preparation instrument IVD

Rapid Detection System by Daan Gene Co., Ltd. — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Nucleic acid sample preparation instrument IVD.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Daan Gene Co., Ltd.
EUDAMED SRN
CN-MF-000025799
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED 97774f5f-423c-427e-a1e3-df9396bc09df 61 fields · synced Jun 18, 2026