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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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Disc Tray — 3 UDI-DI variants, MDR (HumanTech Spine GmbH)

MD Atlas
HumanTech Spine GmbH

Data from EUDAMED, last updated May 31, 2026

Disc Tray

42505399353NK

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: HumanTech Spine GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42505399353NK
Device name: Disc Tray
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 29, 2026

Manufacturer & authorised representative

Manufacturer

Name: HumanTech Spine GmbH
SRN: DE-MF-000010596
Country: Germany
Email: info@humantech-spine.de
Phone: +49 (0) 7157 5246 71

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KSSPXGX0K74TFZTNDQM2BSMK

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

190101030504250539941930
190101030604250539941947
190101030404250539941923