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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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Bone Level Mini Fixture Lab Analog — 284 UDI-DI variants, MDR

MD Atlas
Novodent SA

Data from EUDAMED, last updated May 23, 2026

Bone Level Mini Fixture Lab Analog

764016818003D7

284 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: Novodent SA

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Device characteristics

Administers medicine

Identity & classification

Basic UDI-DI: 764016818003D7
Device name: Bone Level Mini Fixture Lab Analog
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 17, 2024

Manufacturer & authorised representative

Manufacturer

Name: Novodent SA
SRN: CH-MF-000023309
Country: Switzerland
Email: severinecotting@implantswiss.com
Phone: +41 (0) 24 524 2828

Authorised representative

Name: Emergo Europe B.V.
SRN: NL-AR-000000116
Country: Netherlands
Phone: +31 70 345 8570

Variants by status

UDI-DI variants

284 UDI-DI variants

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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

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