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type I

EUDAMED

Class A (EU MDR)

Ref 4×250mL

by Baso Diagnostics Inc. Zhuhai

Identity

Trade Name
type I EUDAMED
Device Name
H-E Stain (H-E) EUDAMED
Model / Reference
4×250mL EUDAMED

Identifiers

Primary DI / UDI-DI
06952383300441 EUDAMED
Basic UDI-DI
695238330015GN EUDAMED
Direct Marketing DI
06952383300441 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

type 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 b3e68f1a-a800-4762-8395-11c6ac88f2db 61 fields · synced Jul 14, 2026