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Genedian

EUDAMED

Class A (EU MDR)

Ref P111-00032Model EB-1000

by Hangzhou DIAN Biotechnology Co., Ltd.

Identity

Trade Name
GENEDIAN EUDAMED
Device Name
Nucleic Acid Extraction System EB1000 EUDAMED
Model / Reference
EB-1000 EUDAMED
P111-00032 EUDAMED

Identifiers

Primary DI / UDI-DI
06934244500153 EUDAMED
Basic UDI-DI
69342445IA004FP EUDAMED
EMDN Code
W02069099 VARIOUS SAMPLE PROCESSING INSTRUMENTS - OTHER EUDAMED

Classification

Device Class
Class A 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

Genedian by Hangzhou DIAN Biotechnology Co., Ltd. — 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

EUDAMED SRN
CN-MF-000007252
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED 6b7ddb7b-4657-464e-b5e6-dbc3f46f167e 61 fields · synced Jun 18, 2026