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Explorer-WHO Probe

EUDAMED

Class I (EU MDR)

Ref 8-550BSIRef 23-550BSI

by LM-Instruments Oy

Identity

Trade Name
Explorer-WHO Probe EUDAMED
Device Name
Diagnostic dental hand instrument EUDAMED
Model / Reference
8-550BSI EUDAMED
23-550BSI EUDAMED

Identifiers

Primary DI / UDI-DI
06438311221236 EUDAMED
06438311209852 EUDAMED
Basic UDI-DI
6438311DIAGNO10QV EUDAMED
Direct Marketing DI
06438311221236 EUDAMED
06438311209852 EUDAMED
EMDN Code
Q0199 ODONTOLOGY 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

Explorer-WHO Probe by LM-Instruments Oy — 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

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

Sources (2)

  • EUDAMED d1bcabb2-d284-4457-b030-b4920e757044 61 fields · synced Jul 30, 2026
  • EUDAMED cfeb5241-0596-4611-b24c-efff9b201286 61 fields · synced May 18, 2026