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TypeⅡ

EUDAMED

Class A (EU MDR)

Ref 100 Tests

by Baso Diagnostics Inc. Zhuhai

Identity

Trade Name
TypeⅡ EUDAMED
Device Name
Immunofluorescence Stain for Genital Secretion EUDAMED
Model / Reference
100 Tests EUDAMED

Identifiers

Primary DI / UDI-DI
06952383304005 EUDAMED
Basic UDI-DI
695238330058H8 EUDAMED
Direct Marketing DI
06952383304005 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

TypeⅡ 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 4cc3e292-3829-4a3e-b218-d823f006fcac 61 fields · synced Jun 19, 2026