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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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PREBOND — 2 UDI-DI variants, MDR (President Dental GmbH)

MD Atlas
President Dental GmbH

Data from EUDAMED, last updated May 23, 2026

PREBOND

426029627BON00132

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: President Dental GmbH

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Device characteristics

Implantable

Identity & classification

Basic UDI-DI: 426029627BON00132
Device name: PREBOND
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
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

basicUdiUlid01K8KE6S2X2FWW5V5XNHDTCNRN

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

PREBOND - Light Cure , Universal Bond 5th Generation 5ml04260296270167
PREBOND SE - Light Cure Self-Etching Universal Bonding 7th Generation 5ml04260296271775