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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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Major Plus, Major Super Lux, Major… — 1 UDI-DI variant, MDR

MD Atlas
Major Prodotti Dentari S.p.A.

Data from EUDAMED, last updated May 30, 2026

Major Plus, Major Super Lux, Major Dent, Bambino tooth

8056640TEEGF

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Major Prodotti Dentari S.p.A.

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: 0425-MDR-030075-01
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: ICIM S.P.A. (0425)
Validity: May 12, 2025 → Apr 18, 2029

Identity & classification

Basic UDI-DI: 8056640TEEGF
Device name: Major Plus, Major Super Lux, Major Dent, Bambino tooth
Device model: Acrylic resin artificial teeth
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 5, 2026

Manufacturer & authorised representative

Manufacturer

Name: Major Prodotti Dentari S.p.A.
SRN: IT-MF-000024700
Country: Italy
Email: angelo.renaldo@majordental.com
Phone: +39 011 6400211

Variants by status

UDI-DI variants

1 UDI-DI variant

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basicUdiUlid01KGQE34056PQBASVWMSBQ3F8P

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

T3011.A1.0/0.L08056640029095