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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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Mobile — 3 UDI-DI variants, MDR (ONCARE GmbH)

MD Atlas
ONCARE GmbH

Data from EUDAMED, last updated May 23, 2026

Mobile

426065886947238412232007H

3 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: ONCARE GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426065886947238412232007H
Device name: Mobile
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 9, 2022

Manufacturer & authorised representative

Manufacturer

Name: ONCARE GmbH
SRN: DE-MF-000007460
Country: Germany
Email: service@myoncare.com
Phone: +49 (0) 89 4445 1156

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01GHDZCF39CC56S09VAMX5SWST

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

myoncare04260658860241
myoncare04260658860227
myoncare04260658860210