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Fungal immunofluorescence chromogenic reagent (Ⅰ)

EUDAMED

Class A (EU MDR)

Ref 100 Tests

by Baso Diagnostics Inc. Zhuhai

Identity

Trade Name
Fungal immunofluorescence chromogenic reagent (Ⅰ) EUDAMED
Device Name
Fungal immunofluorescence chromogenic reagent (Ⅰ) EUDAMED
Model / Reference
100 Tests EUDAMED

Identifiers

Primary DI / UDI-DI
06952383302988 EUDAMED
Basic UDI-DI
695238330024GP EUDAMED
Direct Marketing DI
06952383302988 EUDAMED
EMDN Code
W0103010301 HISTO / CYTO STAINS 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

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Fungal immunofluorescence chromogenic reagent (Ⅰ) by Baso Diagnostics Inc. Zhuhai — 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-000050424
Authorised Representative
Eunitor GmbH DE-AR-000005081

Sources (1)

  • EUDAMED ef1ff797-7bd5-4023-84f6-4f3a61273326 61 fields · synced Jul 22, 2026