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Citotest

EUDAMED

Class I (EU MDR)

Ref 0010-0032Model Plastic shaft

by Citotest Labware Manufacturing Co., Ltd

Identity

Trade Name
CITOTEST EUDAMED
Device Name
Cytology Brushes EUDAMED
Model / Reference
Plastic shaft EUDAMED
0010-0032 EUDAMED

Identifiers

Primary DI / UDI-DI
06975085645351 EUDAMED
Basic UDI-DI
697079159SCDA100A00NDK EUDAMED
EMDN Code
U089002 DEVICES FOR GYNAECOLOGICAL CYTOLOGY EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Citotest by Citotest Labware Manufacturing Co., Ltd — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

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

Sources (1)

  • EUDAMED 4c1b2839-f43f-4509-8fe6-e3f321e3affe 61 fields · synced Jun 19, 2026