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Temporary Model Model T1.0-A1

EUDAMED

Class I (EU MDR)

Ref Model T1.0-A1 Model Model T1.0-A1, Model T1.0-A2, Model T1.0-A3, Model T1.0-A3.5, Model T1.0-A4, Model T1.0-B1, Model T1.0-B2, Model T1.0-B3

by Riton 3D Technology Co., Ltd

Identity

Trade Name
Temporary Model Model T1.0-A1 EUDAMED
Device Name
Temporary Model EUDAMED
Model / Reference
Model T1.0-A1, Model T1.0-A2, Model T1.0-A3, Model T1.0-A3.5, Model T1.0-A4, Model T1.0-B1, Model T1.0-B2, Model T1.0-B3 EUDAMED
Model T1.0-A1 EUDAMED

Identifiers

Primary DI / UDI-DI
06975902950361 EUDAMED
Basic UDI-DI
697590295RXT08X7 EUDAMED
EMDN Code
Q0102050101 TEMPORARY TEETH RESINS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria 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: Dental appliance fabrication material, resin

Temporary Model Model T1.0-A1 by Riton 3D Technology Co., Ltd — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental appliance fabrication material, resin.

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 26cec084-e502-4e64-9ca1-6adc64999c46 61 fields · synced Aug 1, 2026