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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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E Series — 3 UDI-DI variants, MDR (3Shape A/S)

MD Atlas
3Shape A/S

Data from EUDAMED, last updated May 23, 2026

E Series

590272975007F4

3 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: 3Shape A/S

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 590272975007F4
Device name: E Series
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: 3Shape A/S
SRN: DK-MF-000001217
Country: Denmark
Email: regulatory@3shape.com
Phone: +45 70 27 26 20

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KS28EH95DDQTYEJZZTMHA6XJ

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

E405902729752916
E305902729750370
E205902729750363