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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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CEMEL Articulation Paper — 2 UDI-DI variants, MDR

MD Atlas
President Dental GmbH

Data from EUDAMED, last updated May 23, 2026

CEMEL Articulation Paper

426029627ART0014Y

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: President Dental GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426029627ART0014Y
Device name: CEMEL Articulation Paper
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 27, 2025

Manufacturer & authorised representative

Manufacturer

Name: President Dental GmbH
SRN: DE-MF-000014901
Country: Germany
Email: info@presidentdental.com
Phone: +49 8166 3899820

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01K8KKNJE3RV7QP8K0QNA27HZR

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

CEMEL I FORM - Articulating Paper I Form , Red / Blue 12 pcs04260296272673
CEMEL U FORM - Articulating Paper U Form Red / Blue 6 pcs04260296272680