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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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Planmeca Emerald S — 2 UDI-DI variants, MDR (Planmeca Oy)

MD Atlas
Planmeca Oy

Data from EUDAMED, last updated May 23, 2026

Planmeca Emerald S

6430035420205H

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: Planmeca Oy

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 6430035420205H
Device name: Planmeca Emerald S
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 28, 2022

Manufacturer & authorised representative

Manufacturer

Name: Planmeca Oy
SRN: FI-MF-000006499
Country: Finland
Email: niina.vuorikallas@planmeca.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01G6MG5K08V48DPX8H58AMA2WK

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

3003972206430035420902
30018474 06430035420889