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Columbia 2L-2R Orbis

EUDAMED

Class I (EU MDR)

Ref 217-218PDOLMModel Dental hand instrument, curette for the removal of the subgingival and supragingival calculus

by LM-Instruments Oy

Identity

Trade Name
Columbia 2L-2R Orbis EUDAMED
Device Name
Periodontal hand instrument EUDAMED
Model / Reference
Dental hand instrument, curette for the removal of the subgingival and supragingival calculus EUDAMED
217-218PDOLM EUDAMED

Identifiers

Primary DI / UDI-DI
06438311706481 EUDAMED
Basic UDI-DI
B-06438311706481 EUDAMED
6438311PERIO1r06S EUDAMED
Direct Marketing DI
06438311706481 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

Columbia 2L-2R Orbis by LM-Instruments Oy — Class I — MDR, MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

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Manufacturer

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

Sources (2)

  • EUDAMED 08184d3c-0567-4ae1-b054-75496a467a2f 61 fields · synced Jul 12, 2026
  • EUDAMED 702a9f9b-f7cc-48b6-9c05-99a812af1e1e 61 fields · synced May 19, 2026