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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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Knee Brace — 2 UDI-DI variants, MDR (Moovartes BV)

MD Atlas
Moovartes BV

Data from EUDAMED, last updated May 23, 2026

Knee Brace

540700934ABC103PK

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: Moovartes BV

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 540700934ABC103PK
Device name: Knee Brace
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: Moovartes BV
SRN: BE-MF-000004088
Country: Belgium
Email: sophie@moovartes.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KQ7G3FBD87HNRD5WHBE3GFCV

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

S-FIT-80-003-U905407009340659
S-FIT-80-004-U905407009340666