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EXPASYL x20

EUDAMED

Class I (EU MDR)

Ref 261030

by Acteon Manufacturing

Identity

Trade Name
EXPASYL x20 EUDAMED
Device Name
EXPASYL EUDAMED
Model / Reference
261030 EUDAMED

Identifiers

Primary DI / UDI-DI
03760243007026 EUDAMED
Basic UDI-DI
376024300expasyl27 EUDAMED
Unit of Use DI
03760243009808 EUDAMED
EMDN Code
Q010204 RETRACTION WIRES AND GINGIVAL RETRACTORS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France 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

EXPASYL x20 by Acteon Manufacturing — 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

EUDAMED SRN
FR-MF-000007556

Sources (1)

  • EUDAMED 62a6fb39-84e3-44ab-878d-27809b5cb40a 61 fields · synced Jun 18, 2026