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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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Surgical Guide Resins, Photo-Cured — 7 UDI-DI variants, MDR

MD Atlas
Vertex-Dental B.V.

Data from EUDAMED, last updated May 30, 2026

Surgical Guide Resins, Photo-Cured

871942550NDSGA16T6

7 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: Vertex-Dental B.V.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 871942550NDSGA16T6
Device name: —
Device model: Surgical Guide Resins, Photo-Cured
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 25, 2024

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

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01J3MNWM0KDVPW7NGYJ3GY19QN

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

Ceramill SG08719425508818
E - Guide Tint08719425500041
NextDent SG08719425509297
NextDent SG08719425500003
NextDent SG08719425509815
NextDent SG08719425504834
NextDent SG08720604633863