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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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NextDent Base / LT — 1 UDI-DI variant, MDD (Vertex-Dental B.V.)

MD Atlas
Vertex-Dental B.V.

Data from EUDAMED, last updated May 30, 2026

NextDent Base / LT

B-08720604634051

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIa

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Manufacturer: Vertex-Dental B.V.

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: BE19/819943693
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: SGS Belgium NV (1639)
Validity: May 24, 2024

Identity & classification

Basic UDI-DI: B-08720604634051
Device name: NextDent Base / LT
Device model: NDBSLT01000_01
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: Oct 16, 2023

Manufacturer & authorised representative

Manufacturer

Name: Vertex-Dental B.V.
SRN: NL-MF-000019230
Country: Netherlands
Email: info.vertex@3dsystems.com
Phone: +3188616400

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01HCW3GR9A2GHF0GG3A0HVBP9E

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

NextDent Base08720604634051