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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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Movesense Chest Strap MD — 3 UDI-DI variants, MDR (Movesense Ltd)

MD Atlas
Movesense Ltd

Data from EUDAMED, last updated May 23, 2026

Movesense Chest Strap MD

64298108830026M

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: Movesense Ltd

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 64298108830026M
Device name: Movesense Chest Strap MD
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 24, 2025

Manufacturer & authorised representative

Manufacturer

Name: Movesense Ltd
SRN: FI-MF-000024281
Country: Finland
Email: jussi.kaasinen@movesense.com

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01JSK8N6SJ9HNTHT1BT6BZY8ZQ

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

Movesense Chest Strap MD - Size L64298108830492
Movesense Chest Strap MD - Size M64298108830324
Movesense Chest Strap MD - Size S06429810883025