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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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CaseManager DX — 3 UDI-DI variants, IVDR (3DHISTECH Kft.)

MD Atlas
3DHISTECH Kft.

Data from EUDAMED, last updated May 24, 2026

CaseManager DX

599957147155SE

3 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: 3DHISTECH Kft.

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 599957147155SE
Device name: CaseManager DX
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Special device type: refdata.special-ivd-device-type.software
Version date: Jul 13, 2023

Manufacturer & authorised representative

Manufacturer

Name: 3DHISTECH Kft.
SRN: HU-MF-000014337
Country: Hungary
Email: info@3dhistech.com
Phone: +36 1 467 5600

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01H1C05B0MKXYXMECTSZ3DJMQG

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

Case Manager DX05999571470150
CaseManager DX05999571470303
CaseManager DX05999571470297