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Smartcord X 04

EUDAMED

Class I (EU MDR)

Ref EDSX-FModel Smartcord X

by EASTDENT Co., Ltd

Identity

Trade Name
Smartcord X 04 EUDAMED
Device Name
Gingival Retraction Cord EUDAMED
Model / Reference
Smartcord X EUDAMED
EDSX-F EUDAMED

Identifiers

Primary DI / UDI-DI
08809370410332 EUDAMED
Basic UDI-DI
880937041001279 EUDAMED
EMDN Code
Q010204 RETRACTION WIRES AND GINGIVAL RETRACTORS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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: Gingival retraction cord, non-medicated

Smartcord X 04 by EASTDENT Co., Ltd — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Gingival retraction cord, non-medicated.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
EASTDENT Co., Ltd
EUDAMED SRN
KR-MF-000022583
Authorised Representative
KTR Europe GmbH DE-AR-000005685

Sources (1)

  • EUDAMED eed0e40b-edd1-4358-8bf9-67ccdad7225f 61 fields · synced Jun 19, 2026