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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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Cart — 2 UDI-DI variants, MDR (Winncare Nordic)

MD Atlas
Winncare Nordic

Data from EUDAMED, last updated May 31, 2026

Cart

5740008101007SP

2 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: Winncare Nordic

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 5740008101007SP
Device name: Cart
Device model: Luna Mover
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 11, 2025

Manufacturer & authorised representative

Manufacturer

Name: Winncare Nordic
SRN: DK-MF-000002147
Country: Denmark
Email: info@ergolet.dk
Phone: +45 7027 3720

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JR7KE0WE08GG9NMZ9V8GP7C5

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

Winncare05740008102812
Winncare05740008103376