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Anbio

EUDAMED

Class A (EU MDR)

Ref ADL-i1910

by Anbio (Xiamen) Biotechnology Co., Ltd.

Identity

Trade Name
Anbio EUDAMED
Device Name
Automatic Luminescence Immunoassay Analyzer EUDAMED
Model / Reference
ADL-i1910 EUDAMED

Identifiers

Primary DI / UDI-DI
06973861680282 EUDAMED
Basic UDI-DI
6973861680282EW EUDAMED
EMDN Code
W0201020102 AUTOMATED IMMUNOCHEMISTRY ANALYSERS - MODERATE ROUTINE (Throughput > 100 and <= 250 test/h) 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

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

No

EUDAMED

Anbio by Anbio (Xiamen) 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-000023936
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED 41acbbaf-9780-497b-b48b-0fcb5d1c6833 61 fields · synced Jun 18, 2026