Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

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

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Restorative dental hand instrument — 380 UDI-DI variants, MDR

MD Atlas
LM-Instruments Oy

Data from EUDAMED, last updated May 23, 2026

Restorative dental hand instrument

6438311RESTO102Y

380 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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 6438311RESTO102Y
Device name: Restorative dental hand instrument
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

380 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01G2A7NNQEH6X8BCPPDQ057X5W

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

Universal Carver occlusal-proximal06438311219578
Universal Carver occlusal-proximal06438311219561
Universal Carver occlusal-proximal06438311219530
Universal Carver occlusal-proximal DTS06438311030777
Universal Carver occlusal-proximal DTS U06438311030722