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Citotest

EUDAMED

Class I (EU MDR)

Ref 0500-1105Model Mailers

by Citotest Labware Manufacturing Co., Ltd

Identity

Trade Name
CITOTEST EUDAMED
Device Name
Slide Mailers EUDAMED
Model / Reference
Mailers EUDAMED
0500-1105 EUDAMED

Identifiers

Primary DI / UDI-DI
06975085640585 EUDAMED
Basic UDI-DI
697079159MSA1001A00NAZ 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

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 16b27794-a35d-4c34-ae64-6fc4f552f634 61 fields · synced Jun 19, 2026