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Aucheer iRaTe 300 Dry fluorescence immunoassay analyzer

EUDAMED

Class A (EU MDR)

Ref L0300

by Ningbo Aucheer Biotechnology Co., Ltd.

Identity

Trade Name
Aucheer iRaTe 300 Dry fluorescence immunoassay analyzer EUDAMED
Device Name
Aucheer iRaTe 300 Dry fluorescence immunoassay analyzer EUDAMED
Model / Reference
L0300 EUDAMED

Identifiers

Primary DI / UDI-DI
06974546541232 EUDAMED
Basic UDI-DI
0697454654L0300YB EUDAMED
Direct Marketing DI
06974546541232 EUDAMED
EMDN Code
W0201020201 IMMUNOCHEMISTRY READERS 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

Aucheer iRaTe 300 Dry fluorescence immunoassay analyzer by Ningbo Aucheer Biotechnology Co., Ltd. — Class A — IVDR — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
CN-MF-000038081
Authorised Representative
MedPath GmbH DE-AR-000000087

Sources (1)

  • EUDAMED add2d233-a79f-4b48-98d6-711931f2a8a7 61 fields · synced Jun 19, 2026