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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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WALKERS — 3 UDI-DI variants, MDR (NEUSSCARE)

MD Atlas
NEUSSCARE

Data from EUDAMED, last updated May 19, 2026

WALKERS

37017798WALKERSZ6

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: NEUSSCARE

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 37017798WALKERSZ6
Device name: WALKERS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 15, 2025

Manufacturer & authorised representative

Manufacturer

Name: NEUSSCARE
SRN: FR-MF-000044198
Country: France
Email: contact@neuss.care
Phone: +33 5 32 62 96 64

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01K2Q1SWRV9M4FSXKJGZN55JYZ

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

NSC4025W03701779800033
NSC4015A03701779800019
NSC402503701779800095