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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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Steribehälter für MSV-Kit… — 5 UDI-DI variants, MDR

MD Atlas
inomed Medizintechnik GmbH

Data from EUDAMED, last updated May 23, 2026

Steribehälter für MSV-Kit Leksell-Adaption - Elekta

42503076FZS120AU

5 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: inomed Medizintechnik GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42503076FZS120AU
Device name: Steribehälter für MSV-Kit Leksell-Adaption - Elekta
Device model: 230900
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 23, 2025

Manufacturer & authorised representative

Manufacturer

Name: inomed Medizintechnik GmbH
SRN: DE-MF-000005589
Country: Germany
Email: info@inomed.com
Phone: +49764194140

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01K88HVMA1WJHVNCSDX02QGS46

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

Quiver, safe-keeping tube for electrode04250307600762
Sterilisation box for MicroDrive kit - Elekta04250307600724
Sterilisation box for MicroDrive kit Leksell04250307600748
Sterilisation box for MicroDrive kit Micromar04250307600755
Sterilisation box for MicroDrive Kit ZD/RM/CRW04250307600731