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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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JiveX — 6 UDI-DI variants, MDR (VISUS Health IT GmbH)

MD Atlas
VISUS Health IT GmbH

Data from EUDAMED, last updated May 23, 2026

JiveX

426063247JiveXMV

6 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: VISUS Health IT GmbH

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 426063247JiveXMV
Device name: JiveX
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: May 22, 2024

Manufacturer & authorised representative

Manufacturer

Name: VISUS Health IT GmbH
SRN: DE-MF-000005585
Country: Germany
Email: info@visus.com
Phone: +49234936930

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01HGDHWXK9H549BF38CP6EGA9K

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

JiveX04260632470107
JiveX 5.4.0.18+04260632470077
JiveX04260632470114
JiveX 5.704260632470121
JiveX 5.804260632470138
JiveX 5.3.0.40+04260632470046