← Back to catalogue

Citotest

EUDAMED

Class I (EU MDR)

Ref 2123-1003Model Nylon

by Citotest Labware Manufacturing Co., Ltd

Identity

Trade Name
CITOTEST EUDAMED
Device Name
Classical swabs EUDAMED
Model / Reference
Nylon EUDAMED
2123-1003 EUDAMED

Identifiers

Primary DI / UDI-DI
06975085648864 EUDAMED
Basic UDI-DI
697079159SWA1000B00RLK EUDAMED
EMDN Code
A1101 SAMPLE COLLECTION NEUTRAL SWABS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Türkiye EUDAMED

Clinical & Handling

Sterile

Yes

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-purpose absorbent tip applicator/swab, single-use

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

Similar devices

Also classified as General-purpose absorbent tip applicator/swab, single-use.

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 d9f477a1-0d9e-4141-95c5-d0c15b47c942 61 fields · synced Jun 19, 2026