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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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MoVeS Buck Hammer — 5 UDI-DI variants, MDR (MVS In Motion)

MD Atlas
MVS In Motion

Data from EUDAMED, last updated May 23, 2026

MoVeS Buck Hammer

542006300J3H

5 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: MVS In Motion

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 542006300J3H
Device name: MoVeS Buck Hammer
Device model: Neurological Hammers
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 18, 2024

Manufacturer & authorised representative

Manufacturer

Name: MVS In Motion
SRN: BE-MF-000000664
Country: Belgium
Email: info@mvs-in-motion.com

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01J0NR501DQ3S0KR9V0F19QJQ2

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

08-05010205420063004534
08-05010105420063004527
08-05010405420063004862
08-05010305420063004541
08-05010505420063004879