← Back to catalogue

Citotest

EUDAMED

Class I (EU MDR)

Ref 0410-0009Model Glass

by Citotest Labware Manufacturing Co., Ltd

Identity

Trade Name
CITOTEST EUDAMED
Device Name
Staining Jar EUDAMED
Model / Reference
Glass EUDAMED
0410-0009 EUDAMED

Identifiers

Primary DI / UDI-DI
06975085641735 EUDAMED
Basic UDI-DI
697079159MSA1002A00NBC EUDAMED
EMDN Code
W05030599 DEVICES FOR PATOLOGY TESTS - OTHER 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 — CE/MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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 25152dea-8d04-4b80-94f4-04b4ac730fbc 61 fields · synced Oct 6, 2026