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Citotest

EUDAMED

Class I (EU MDR)

Ref 0510-0002-10Model Plastic

by Citotest Labware Manufacturing Co., Ltd

Identity

Trade Name
CITOTEST EUDAMED
Device Name
Storage Cabinet EUDAMED
Model / Reference
Plastic EUDAMED
0510-0002-10 EUDAMED

Identifiers

Primary DI / UDI-DI
06975085641827 EUDAMED
Basic UDI-DI
697079159SSDA000B00NTR EUDAMED
EMDN Code
W050299 DEVICES FOR SAMPLES TRANSPORT - 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

Category: General specimen container IVD, no additive/medium

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

Similar devices

Also classified as General specimen container IVD, no additive/medium.

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 93685715-0748-4e9b-bab9-4a0643312b75 61 fields · synced Jun 18, 2026