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Mls

EUDAMED

Class A (EU MDR)

Ref A202541Model Plastic

by Citotest Labware Manufacturing Co., Ltd

Identity

Trade Name
MLS EUDAMED
Device Name
Specimen Container EUDAMED
Model / Reference
Plastic EUDAMED
A202541 EUDAMED

Identifiers

Primary DI / UDI-DI
06942826211588 EUDAMED
Basic UDI-DI
697079159ASCA002A00NA3 EUDAMED
EMDN Code
W05020199 SAMPLES TRANSPORT, CONTAINERS - OTHER 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

Mls 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

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Manufacturer

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

Sources (1)

  • EUDAMED 61906d0c-a7af-4431-b01f-e99644250955 61 fields · synced Jul 24, 2026