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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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LM-OrthoSizer™ is a tool for aiding… — 2 UDI-DI variants, MDR

MD Atlas
LM-Instruments Oy

Data from EUDAMED, last updated May 23, 2026

LM-OrthoSizer™ is a tool for aiding the selection of the appropriate LM-Activator™ size.

6438311ORTHOSIZER10GC

2 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: LM-Instruments Oy

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 6438311ORTHOSIZER10GC
Device name: LM-OrthoSizer™ is a tool for aiding the selection of the appropriate LM-Activator™ size.
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 5, 2022

Manufacturer & authorised representative

Manufacturer

Name: LM-Instruments Oy
SRN: FI-MF-000006705
Country: Finland
Email: info@lm-dental.com
Phone: +358 2 4546 400

Variants by status

UDI-DI variants

2 UDI-DI variants

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basicUdiUlid01G2AKCHMTS93C67EGR8MBJVYK

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

LM-Activator 2 OrthoSizer06438311221908
LM-OrthoSizer06438311221847