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DuoSculpt

EUDAMED

Class I (EU MDR)

Ref 473-753XSIGC

by LM-Instruments Oy

Identity

Trade Name
DuoSculpt EUDAMED
Device Name
Restorative dental hand instrument EUDAMED
Model / Reference
473-753XSIGC EUDAMED

Identifiers

Primary DI / UDI-DI
06438311708683 EUDAMED
Basic UDI-DI
6438311RESTO102Y EUDAMED
Direct Marketing DI
06438311708683 EUDAMED
EMDN Code
Q01010199 DENTAL RESTORATION DEVICES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Finland 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, ceramic

DuoSculpt by LM-Instruments Oy — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Dental appliance fabrication material, ceramic.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
LM-Instruments Oy
EUDAMED SRN
FI-MF-000006705

Sources (1)

  • EUDAMED 97e0295a-c82a-4ebd-8f11-b2324e409223 61 fields · synced Jun 18, 2026