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Dental Model Model V1.0-G

EUDAMED

Class I (EU MDR)

Ref Model V1.0-GModel Model V1.0-G/Model V1.0-Y/Model W1.0-B/Model H1.0-G/Model H1.0-Y/Model S1.0-G/Model S1.0-Y

by Riton 3D Technology Co., Ltd

Identity

Trade Name
Dental Model Model V1.0-G EUDAMED
Device Name
Dental Model EUDAMED
Model / Reference
Model V1.0-G/Model V1.0-Y/Model W1.0-B/Model H1.0-G/Model H1.0-Y/Model S1.0-G/Model S1.0-Y EUDAMED
Model V1.0-G EUDAMED

Identifiers

Primary DI / UDI-DI
06975902950149 EUDAMED
Basic UDI-DI
697590295RXT02WT EUDAMED
EMDN Code
Q01020199 DENTAL IMPRESSION MATERIALS - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Spain 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: Silicone dental impression material

Dental Model Model V1.0-G by Riton 3D Technology Co., Ltd — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Silicone dental impression material.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000044171
Authorised Representative
RIOMAVIX SOCIEDAD LIMITADA ES-AR-000001202

Sources (1)

  • EUDAMED 96bff451-ea49-4c29-800c-6f2c0b64470e 61 fields · synced Jun 18, 2026