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DNA purification reagents

EUDAMED

Class A (EU MDR)

Ref M202506Model MK-DPR

by Aixgen Technology (Heze) Co., Ltd.

Identity

Device Name
DNA purification reagents EUDAMED
Model / Reference
MK-DPR EUDAMED
M202506 EUDAMED

Identifiers

Primary DI / UDI-DI
06978543820024 EUDAMED
Basic UDI-DI
6978543820024F6 EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Spain 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

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Category: Device sterilization/disinfection container, reusable

DNA purification reagents by Aixgen Technology (Heze) Co., Ltd. — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
CN-MF-000047605
Authorised Representative
RIOMAVIX SOCIEDAD LIMITADA ES-AR-000001202

Sources (1)

  • EUDAMED b243f331-1c0b-4bb7-b67d-eb5cb750d763 61 fields · synced Jun 17, 2026