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Citotest

EUDAMED

Class A (EU MDR)

Ref 0200-0008Model white particles

by Citotest Labware Manufacturing Co., Ltd

Identity

Trade Name
CITOTEST EUDAMED
Device Name
Paraffin Wax EUDAMED
Model / Reference
white particles EUDAMED
0200-0008 EUDAMED

Identifiers

Primary DI / UDI-DI
06970791591978 EUDAMED
Basic UDI-DI
697079159EBMA000A00N52 EUDAMED
EMDN Code
W01030704 EMBEDDING MEDIA (HISTOLOGY/CYTOLOGY) EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Austria 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

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Citotest by Citotest Labware Manufacturing Co., Ltd — Class A — CE/MDR — 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-000017214
Authorised Representative
Obelis s.a. BE-AR-000000106

Sources (1)

  • EUDAMED 858e148e-46a6-4af5-8f41-16426ba69f3b 61 fields · synced Oct 6, 2026