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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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VibroSense Meter II — 1 UDI-DI variant, MDR (VibroSense Dynamics AB)

MD Atlas
VibroSense Dynamics AB

Data from EUDAMED, last updated May 31, 2026

VibroSense Meter II

735018150VSMIIDV

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: VibroSense Dynamics AB

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Device characteristics

Measuring function

Identity & classification

Basic UDI-DI: 735018150VSMIIDV
Device name: VibroSense Meter II
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 29, 2026

Manufacturer & authorised representative

Manufacturer

Name: VibroSense Dynamics AB
SRN: SE-MF-000003787
Country: Sweden
Email: info@vibrosense.com
Phone: +464088026

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01K62V1AKPEV3W9EB4HGBCPGJ4

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

VibroSense Meter II07350181500008