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Denture Base Model D1.0-LP

EUDAMED

Class I (EU MDR)

Ref Model D1.0-LPModel Model D1.0-DP /Model D1.0-LP/ Model F1.0-T/ Model F1.0-TP /Model O1.0-T/ Model O1.0-TP

by Riton 3D Technology Co., Ltd

Identity

Trade Name
Denture Base Model D1.0-LP EUDAMED
Device Name
Denture Base EUDAMED
Model / Reference
Model D1.0-DP /Model D1.0-LP/ Model F1.0-T/ Model F1.0-TP /Model O1.0-T/ Model O1.0-TP EUDAMED
Model D1.0-LP EUDAMED

Identifiers

Primary DI / UDI-DI
06975902950200 EUDAMED
Basic UDI-DI
0697590295RXT06J9 EUDAMED
EMDN Code
Q0102050102 DENTAL REBASING RESINS 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

Denture Base Model D1.0-LP by Riton 3D Technology Co., Ltd — 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

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

Sources (1)

  • EUDAMED 75db9cf2-c69b-4c7a-a6cd-841909b86d98 61 fields · synced Jun 19, 2026