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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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SkinNeutrAll — 5 UDI-DI variants, MDR (Vebasan OÜ)

MD Atlas
Vebasan OÜ

Data from EUDAMED, last updated May 23, 2026

SkinNeutrAll

4280001912BodyNeutrAll2FU

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: Vebasan OÜ

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4280001912BodyNeutrAll2FU
Device name: SkinNeutrAll
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 5, 2024

Manufacturer & authorised representative

Manufacturer

Name: Vebasan OÜ
SRN: EE-MF-000043782
Country: Estonia
Email: info@vebasan.com
Phone: +491759144607

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01J9E6AR2GEY2F29JJNEENZE89

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

EST 0030004280001912052
EST 0030004280001912212
EST 0010004280001912106
EST 0100 x 404262471880246
EST 0100 Bottle 204262471880222