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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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Wart & Verruca Gel Treatment, Wart &… — 2 UDI-DI variants, MDR

MD Atlas
Unigroup ApS

Data from EUDAMED, last updated May 23, 2026

Wart & Verruca Gel Treatment, Wart & Verruca Treatment, Molluscum Treatment, Foot Corn Treatment

57064481010KERATOLYTICJX

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Unigroup ApS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 57064481010KERATOLYTICJX
Device name: Wart & Verruca Gel Treatment, Wart & Verruca Treatment, Molluscum Treatment, Foot Corn Treatment
Device model: Keratolytic
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jan 23, 2026

Manufacturer & authorised representative

Manufacturer

Name: Unigroup ApS
SRN: DK-MF-000009459
Country: Denmark
Email: info@unigroup.dk
Phone: +4570222818

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KFNEAG87A8G6ZPQ3KRM6QG1F

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

10103505706448000767
10103508720674247793