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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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Try-in Pastes — 29 UDI-DI variants, MDR (Ivoclar Vivadent AG)

MD Atlas
Ivoclar Vivadent AG

Data from EUDAMED, last updated May 31, 2026

Try-in Pastes

76152082AACCE0048R

29 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: Ivoclar Vivadent AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 76152082AACCE0048R
Device name: Try-in Pastes
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: Ivoclar Vivadent AG
SRN: LI-MF-000000522
Country: Liechtenstein
Email: Sandro.Sbicego@ivoclar.com

Variants by status

UDI-DI variants

29 UDI-DI variants

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Applied filters

basicUdiUlid01KS2B5FRM8P72SC8TYRSGP363

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

Variolink N-Esth Try Ref. 1.7g warm+07615208590715
Variolink N-Esth Try Ref. 1.7g warm+07615208590708
Variolink N-Esth Try Ref. 1.7g white o.07615208590685
Variolink N-Esth Try Ref. 1.7g white o.07615208590692

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