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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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Myra Skin YU — 3 UDI-DI variants, MDR (Lifelike Prosthetics GmbH)

MD Atlas
Lifelike Prosthetics GmbH

Data from EUDAMED, last updated May 23, 2026

Myra Skin YU

426255255TrueSkinQK

3 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: Lifelike Prosthetics GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426255255TrueSkinQK
Device name: Myra Skin YU
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 30, 2026

Manufacturer & authorised representative

Manufacturer

Name: Lifelike Prosthetics GmbH
SRN: DE-MF-000049303
Country: Germany
Email: info@lifelike-prosthetics.de
Phone: +49 3371 4045404

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KMZACH812KPMRWF015FJN4N1

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

TS-MS-11004262552550006
TS-MS-12004262552550020
TS-MS-20004262552550051