← Back to catalogue

Citotest

EUDAMED

Class A (EU MDR)

Ref 0103-1103-02Model P.O.M

by Citotest Labware Manufacturing Co., Ltd

Identity

Trade Name
CITOTEST EUDAMED
Device Name
Embedding Cassettes EUDAMED
Model / Reference
P.O.M EUDAMED
0103-1103-02 EUDAMED

Identifiers

Primary DI / UDI-DI
06942826210567 EUDAMED
Basic UDI-DI
697079159TECA000A00NF4 EUDAMED
EMDN Code
W05030501 INCLUSION DEVICES, CASSETTES 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 — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000017214
Authorised Representative
Wellkang Ltd XI-AR-000001836

Sources (1)

  • EUDAMED b4c79c9a-7e04-42f9-a912-cb7835ee3299 61 fields · synced Jun 19, 2026