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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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Kiber Assistant - Android — 2 UDI-DI variants, MDR (VRMEDIA SRL)

MD Atlas
VRMEDIA SRL

Data from EUDAMED, last updated May 30, 2026

Kiber Assistant - Android

805744008KASK4

2 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: VRMEDIA SRL

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805744008KASK4
Device name: Kiber Assistant - Android
Device model: Kiber Assistant
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Special device type: refdata.special-mdr-device-type.software
Version date: May 11, 2026

Manufacturer & authorised representative

Manufacturer

Name: VRMEDIA SRL
SRN: IT-MF-000054046
Country: Italy
Email: info@vrmedia.it
Phone: +39 050 7846933

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KRB33CZZ2ZDSY5876JMPAED0

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

KAS-I80574400800196
KAS-A80574400800028