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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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Neolook One — 3 UDI-DI variants, MDR (Neolook Solutions)

MD Atlas
Neolook Solutions

Data from EUDAMED, last updated May 30, 2026

Neolook One

8720299NLONE6F

3 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: Neolook Solutions

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 8720299NLONE6F
Device name: Neolook One
Device model: Neolook One
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: Neolook Solutions
SRN: NL-MF-000028851
Country: Netherlands
Email: hello@neolooksolutions.com
Phone: +3163949555

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KK4BHPJC0N1NQ0JE6S5P1T1A

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

Neolook Compact08720299947764
Neolook One08720299947771
ONE-PRD-40108720299947757