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Mls

EUDAMED

Class A (EU MDR)

Ref H10019Model Pipette

by Citotest Labware Manufacturing Co., Ltd

Identity

Trade Name
MLS EUDAMED
Device Name
Pasteur Pipette EUDAMED
Model / Reference
Pipette EUDAMED
H10019 EUDAMED

Identifiers

Primary DI / UDI-DI
06942826211656 EUDAMED
Basic UDI-DI
697079159STTA000A00N82 EUDAMED
EMDN Code
W0503020199 PIPETTES - 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 49f08b26-f39f-40bf-88a6-73e5a24fdfbb 61 fields · synced Jul 31, 2026