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Immunofluorescence Reader

EUDAMED

Class A (EU MDR)

Ref F6101Model UNICELL-S

by Shenzhen Yhlo Biotech Co., Ltd.

Identity

Device Name
Immunofluorescence Reader EUDAMED
Model / Reference
UNICELL-S EUDAMED
F6101 EUDAMED

Identifiers

Primary DI / UDI-DI
06925912711063 EUDAMED
Basic UDI-DI
692591270143H8 EUDAMED
EMDN Code
W0201069099 VARIOUS RAPID TEST CHEMISTRY / IMMUNOCHEMISTRY INSTRUMENTS - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Greece 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

Immunofluorescence Reader by Shenzhen Yhlo Biotech 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-000001137
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 29140136-4333-4e01-b12e-3225c7e60494 61 fields · synced Jul 13, 2026