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Roeko-Strip

EUDAMED

Class I (EU MDR)

Ref 600009

by Polydentia SA

Identity

Trade Name
Roeko-Strip EUDAMED
Device Name
Roeko-Strip EUDAMED
Model / Reference
600009 EUDAMED

Identifiers

Primary DI / UDI-DI
+E2996000090 EUDAMED
Basic UDI-DI
++E299ROEKOSTRIPLM EUDAMED
EMDN Code
Q01010401 PAPER AND GUTTA-PERCHA TIPS, MATRICES AND WEDGES FOR DENTISTRY 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

Roeko-Strip by Polydentia SA — 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

Manufacturer
Polydentia SA
EUDAMED SRN
CH-MF-000008779
Authorised Representative
IDD International Dental Distributors AG LI-AR-000008367

Sources (1)

  • EUDAMED 70808b9b-cfd7-44f3-8bef-f337964be31a 61 fields · synced Jun 18, 2026