← Back to catalogue

Syntette Mini Orbis

EUDAMED

Class I (EU MDR)

Ref 215-216MPDOLMModel Dental hand instrument, curette for the removal of the subgingival and supragingival calculus

by LM-Instruments Oy

Identity

Trade Name
Syntette Mini Orbis EUDAMED
Device Name
Periodontal hand instrument EUDAMED
Model / Reference
215-216MPDOLM EUDAMED
Dental hand instrument, curette for the removal of the subgingival and supragingival calculus EUDAMED

Identifiers

Primary DI / UDI-DI
06438311706535 EUDAMED
Basic UDI-DI
6438311PERIO1r06S EUDAMED
B-06438311706535 EUDAMED
Direct Marketing DI
06438311706535 EUDAMED
EMDN Code
L159001 DENTAL AND PERIODONTAL CURETTES, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Finland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Syntette Mini Orbis by LM-Instruments Oy — Class I — MDD, MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (2)

  • EUDAMED 3191940a-bc4e-400c-ac66-6339b9c14573 61 fields · synced Aug 5, 2026
  • EUDAMED 057d09c7-0f97-42e4-8e43-4786403c37b0 61 fields · synced May 19, 2026