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Smartcord 02

EUDAMED

Class I (EU MDR)

Ref EDSC-BModel SmartcordRef EDSX-BModel Smartcord X

by EASTDENT Co., Ltd

Identity

Trade Name
Smartcord 02 EUDAMED
Smartcord X 02 EUDAMED
Device Name
Gingival Retraction Cord EUDAMED
Model / Reference
Smartcord EUDAMED
EDSC-B EUDAMED
Smartcord X EUDAMED
EDSX-B EUDAMED

Identifiers

Primary DI / UDI-DI
08809370410066 EUDAMED
08809370410226 EUDAMED
Basic UDI-DI
880937041001177 EUDAMED
880937041001279 EUDAMED
EMDN Code
Q010204 RETRACTION WIRES AND GINGIVAL RETRACTORS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Poland EUDAMED
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 02 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 (2)

  • EUDAMED dcafb403-7e8e-41a7-a9ca-40605ffea973 61 fields · synced Jul 25, 2026
  • EUDAMED 1fed0d37-3c12-49c9-803d-e38ddaa8dfbb 61 fields · synced Jul 9, 2026