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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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SkinScreener v3 — 4 UDI-DI variants, MDR (medaia GmbH)

MD Atlas
medaia GmbH

Data from EUDAMED, last updated May 23, 2026

SkinScreener v3

912011561SKSC354

4 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: medaia GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 912011561SKSC354
Device name: SkinScreener v3
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Nov 27, 2024

Manufacturer & authorised representative

Manufacturer

Name: medaia GmbH
SRN: AT-MF-000011199
Country: Austria
Email: office@medaia.at

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01H1467D99JNV16YA1ZYV4F3F3

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

SkinScreener v3.009120115610077
SkinScreener v3.109120115610107
SkinScreener v3.109120115610114
SkinScreener v3.0 Android09120115610084