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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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neo315 — 2 UDI-DI variants, MDR (Neoscan Solutions GmbH)

MD Atlas
Neoscan Solutions GmbH

Data from EUDAMED, last updated May 23, 2026

neo315

426068559NEO315AL

2 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: Neoscan Solutions GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426068559NEO315AL
Device name: neo315
Device model: neo315
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jul 26, 2023

Manufacturer & authorised representative

Manufacturer

Name: Neoscan Solutions GmbH
SRN: DE-MF-000007899
Country: Germany
Email: info@neoscan-solutions.com
Phone: 039156398541

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01H6904ZGH0ZRK6GVCXV651M6R

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

neo31542606855900128
neo31542606855900050