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Re-Cord

EUDAMED

Class I (EU MDR)

Ref WP4916Model Retraction Cord

by Dent-A-Pharm Produktionsgesellschaft mbH

Identity

Trade Name
Re-Cord EUDAMED
Model / Reference
Retraction Cord EUDAMED
WP4916 EUDAMED

Identifiers

Primary DI / UDI-DI
+D932WP49161H EUDAMED
Basic UDI-DI
++D932RetrCordSA EUDAMED
Direct Marketing DI
+D932WP49161H 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

Re-Cord by dent a pharm Produktionsgesellschaft mbH — 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
DE-MF-000012922

Sources (1)

  • EUDAMED 4bb15e0d-17a8-41cf-8092-135367e51837 61 fields · synced Jul 22, 2026