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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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Vibrosonic alpha Refill Pack Ear Canal… — 5 UDI-DI variants, MDR

MD Atlas
Vibrosonic GmbH

Data from EUDAMED, last updated May 23, 2026

Vibrosonic alpha Refill Pack Ear Canal Modules (for Sizing)

426070005FICV002VD

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: Vibrosonic GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426070005FICV002VD
Device name: Vibrosonic alpha Refill Pack Ear Canal Modules (for Sizing)
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: Vibrosonic GmbH
SRN: DE-MF-000022006
Country: Germany
Email: info@vibrosonic.com
Phone: +49 621 1806269 0

Variants by status

UDI-DI variants

5 UDI-DI variants

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basicUdiUlid01KHY2K2069KQA0ACEFP0VHNMJ

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

FICV002-L04260700050330
FICV002-M04260700050309
FICV002-S04260700050323
FICV002-XL04260700050347
FICV002-XS04260700050316