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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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Bluephase N M / Bluephase N MC — 5 UDI-DI variants, MDR

MD Atlas
Ivoclar Vivadent AG

Data from EUDAMED, last updated May 31, 2026

Bluephase N M / Bluephase N MC

76152081XLAMP002YF

5 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: Ivoclar Vivadent AG

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 76152081XLAMP002YF
Device name: Bluephase N M / Bluephase N MC
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 11, 2025

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

5 UDI-DI variants

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Applied filters

basicUdiUlid01K9RVWYCMW9D2158CRFBKHB61

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

Bluephase N MC 100-240V07615208458886
Bluephase N MC 100-240V07615208458909
Bluephase N MC 100-240V07615208458893
Bluephase N MC 100-240V07615208458916
Bluephase N MC handpiece07615208485059